Search Results (67)

In the context of critical challenges in curcumin-modified polyurethane synthesis—including limited curcumin bioavailability and suboptimal biodegradability/biocompatibility—a novel polyurethane material (Cur-PU) with good mechanical, shape memory, pH-responsive, and biocompatibility was synthesized via a one-pot, two-step synthetic protocol in which HO-PCL-OH served as the soft segment and curcumin was employed as the chain extender. The experimental results demonstrate that with the increase in Cur units, the crystallinity of the Cur-PU material decreases from 32.6% to 5.3% and that the intensities of the diffraction peaks at 2θ = 21.36°, 21.97°, and 23.72° in the XRD pattern gradually diminish. Concomitantly, tensile strength decreased from 35.5 MPa to 19.3 MPa, and Shore A hardness declined from 88 HA to 65 HA. These observations indicate that the sterically hindered benzene ring structure of Cur imposes restrictions on HO-PCL-OH crystallization, leading to lower crystallinity and retarded crystallization kinetics in Cur-PU. As a consequence, the material’s tensile strength and hardness are diminished. Except for the Cur-PU-3 sample, all other variants exhibited exceptional shape-memory functionality, with R_f and R_r exceeding 95%, as determined by three-point bending method. Analogous to pure curcumin solutions, Cur-PU solutions demonstrated pH-responsive chromatic transitions: upon addition of hydroxide ion (OH⁻) solutions at increasing concentrations, the solutions shifted from yellow-green to dark green and finally to orange-yellow, enabling sensitive pH detection across alkaline gradients. Hydrolytic degradation studies conducted over 15 weeks in air, UPW, and pH 6.0/8.0 phosphate buffer solutions revealed mass loss <2% for Cur-PU films. Surface morphological analysis showed progressive etching with the formation of micro-to-nano-scale pores, indicative of a surface-erosion degradation mechanism consistent with pure PCL. Biocompatibility assessments via L929 mouse fibroblast co-culture experiments demonstrated ≥90% cell viability after 72 h, while relative red blood cell hemolysis rates remained below 5%. Collectively, these findings establish Cur-PU as a biocompatible material with tunable mechanical properties, and pH responsiveness, underscoring its translational potential for biomedical applications such as drug delivery systems and tissue engineering scaffolds. Full article

Group IV element-based topological semimetals (TSMs) are pivotal for next-generation quantum devices due to their ultra-high carrier mobility and low-energy consumption. However, germanium (Ge)-based TSMs remain underexplored despite their compatibility with existing semiconductor technologies. Here, we propose a novel I229-Ge₄₈ allotrope constructed via bottom-up cluster assembly that exhibits a unique porous spherical Fermi surface and strain-tunable topological robustness. First-principles calculations reveal that I229-Ge₄₈ is a topological nodal line semimetal with exceptional mechanical anisotropy (Young’s modulus ratio: 2.27) and ductility (B/G = 2.21, ν = 0.30). Remarkably, the topological property persists under spin-orbit coupling (SOC) and tensile strain, while compressive strain induces a semiconductor transition (bandgap: 0.29 eV). Furthermore, I229-Ge₄₈ demonstrates strong visible-light absorption (10⁵ cm⁻¹) and a strong strain-modulated infrared response, surpassing conventional Ge allotropes. These findings establish I229-Ge₄₈ as a multifunctional platform for strain-engineered nanoelectronics and optoelectronic devices. Full article

Polyvinyl alcohol (PVA) hydrogels have emerged as versatile materials due to their exceptional biocompatibility and tunable mechanical properties, showing great promise for flexible sensors, smart wound dressings, and tissue engineering applications. However, rational design remains challenging due to complex structure–property relationships involving multiple formulation parameters. This study presents an interpretable machine learning framework for predicting PVA hydrogel tensile strain properties with emphasis on mechanistic understanding, based on a comprehensive dataset of 350 data points collected from a systematic literature review. XGBoost demonstrated superior performance after Optuna-based optimization, achieving R² values of 0.964 for training and 0.801 for testing. SHAP analysis provided unprecedented mechanistic insights, revealing that PVA molecular weight dominates mechanical performance (SHAP importance: 84.94) through chain entanglement and crystallization mechanisms, followed by degree of hydrolysis (72.46) and cross-linking parameters. The interpretability analysis identified optimal parameter ranges and critical feature interactions, elucidating complex non-linear relationships and reinforcement mechanisms. By addressing the “black box” limitation of machine learning, this approach enables rational design strategies and mechanistic understanding for next-generation multifunctional hydrogels. Full article

A series of para-trifluoromethoxy-substituted and fluorobenzhydryl-functionalized 1,2-bis(imine)acenaphthene ligands: 1-[2,6-{(4-F-C₆H₄)₂CH}₂-4-F₃COC₆H₂N]-2-(ArN)C₂C₁₀H₆ (Ar = 2,6-Me₂C₆H₃ L1, 2,6-Et₂C₆H₃ L2, 2,6-iPr₂C₆H₃ L3, 2,4,6-Me₃C₆H₂ L4, 2,6-Et₂-4-MeC₆H₂ L5), were synthesized and used to generate their corresponding nickel(II) bromide complexes (Ni1–Ni5). Elemental analysis, ¹⁹F NMR, and FT-IR spectroscopy were employed to characterize these five nickel complexes. Single-crystal X-ray diffraction of Ni2 and Ni4 confirmed distorted tetrahedral geometries. Upon activation with either EtAlCl₂ (ethylaluminum dichloride) or EASC (ethyl aluminum sesquichloride), these complexes showed exceptional high activities (up to 22.0 × 10⁶ g PE mol⁻¹ (Ni) h⁻¹) and remarkable thermal stability (4.82 × 10⁶ g PE mol⁻¹(Ni) h⁻¹ at 80 °C) towards ethylene polymerization. The resulting polyethylenes are highly branched, with the type and extent of branches tunable by temperature, solvent, and co-catalyst choice. Moreover, these polymers demonstrated excellent tensile strength (σ_b up to 20.7 MPa) and elastic recovery (up to 58%), characteristic of thermoplastic elastomers (TPEs). These results highlight the dual role of trifluoromethoxy and fluorobenzhydryl groups in enhancing catalytic performance and polymer properties. Full article

Novel three-dimensional porous composites of alginate–pectin (A/P) with zinc- or manganese-substituted hydroxyapatites (A/P-ZnHA and A/P-MnHA) were synthesized via lyophilization and calcium cross-linking. Powder X-ray diffraction and infrared spectroscopy analyses confirmed single-phase apatite formation (crystallite sizes < 1 µm), with ZnHA exhibiting lattice contraction (*c*-axis: 6.881 Å vs. 6.893 Å for HA). Mechanical testing revealed tunable properties: pristine A/P sponges exhibited an elastic modulus of 4.7 MPa and a tensile strength of 0.10 MPa, reduced by 30–70% by HA incorporation due to increased porosity (pore sizes: 112 ± 18 µm in the case of MnHA vs. 148 ± 23 µm-ZnHA). Swelling capacity increased 2.3–2.8-fold (125–155% vs. 55% for A/P), governed by polysaccharide interactions. Scanning electron microscopy investigation showed microstructural evolution from layered A/P (<100 µm) to tridimensional architectures with embedded mineral particles. The A/P-MnHA composites demonstrated minimal cytotoxicity for the NCTC cells and good viability of dental pulp stem cells, while A/P-ZnHA caused ≈20% metabolic suppression, attributed to hydrolysis-induced acidification. Antibacterial assays highlighted A/P-MnHA′s broad-spectrum efficacy against Gram-positive (Bacillus atrophaeus) and Gram-negative (Pseudomonas protegens) strains, whereas A/P-ZnHA targeted only the Gram-positive strain. The developed composite sponges combine cytocompatibility and antimicrobial activity, potentially advancing osteoplastic materials for bone regeneration and infection control in orthopedic/dental applications. Full article

Silicon nitride (SiN) films deposited via plasma-enhanced chemical vapor deposition (PECVD) exhibit tunable tensile stress, which is critical for various microelectronic and optoelectronic applications. In this paper, the effects of silane (SiH₄) flow rate during PECVD deposition, ultraviolet (UV) curing, and layered deposition on the tensile stress of SiN films are mainly investigated. The results reveal that increasing the SiH₄ concentration raises hydrogen incorporation, which modifies internal stress dynamics. UV curing significantly increases tensile stress by breaking N-H and Si-H bonds, facilitating hydrogen desorption, and promoting Si-N-Si crosslinking. The optimal UV curing duration stabilizes tensile stress at approximately 1570 MPa, while excessive UV power alters hydrogen content dynamics, reducing stress. Additionally, layered deposition further amplifies stress enhancement, with films subjected to multiple deposition cycles exhibiting increased densification and crosslinking. The combined optimization of PECVD deposition parameters, UV curing, and layered deposition provides a robust strategy for tailoring SiN film stress, offering a versatile approach to engineering mechanical properties for advanced applications. Full article

Polybenzimidazole (PBI), a high-performance polymer known for its exceptional thermal stability and chemical resistance, was processed by solution electrospinning to manufacture fibrous non-woven membranes. The process was repeated under different conditions by adjusting four main settings: the polymer solution concentration, the flow rate, the voltage applied between the needle and the collector, and the separating distance. To clarify the interplay between process parameters and material properties, a Design of Experiment (DOE) approach was used to systematically analyze the effects of said parameters on microstructural properties, including fiber diameter, porosity, and air permeability, pointing out that the increase in viscosity improves fiber uniformity, while optimizing the applied voltage and the needle–collector distance enhances jet stability and solvent evaporation, crucial for defect-free fibrous microstructures. Post-processing via calendering further refined the membrane texture and properties, for example by reducing porosity and air permeability without significantly altering the fibrous morphology, particularly at low lamination ratios. Thermal and mechanical evaluations highlighted that the obtained electrospun PBI membranes exhibited enhanced flexibility, but lower tensile strength compared to cast films due to the underlying open pore microstructure. This integrated approach—combining experimental characterization, DOE-guided optimization, and post-processing via calendering—provides a systematic framework for tailoring PBI membranes for specific applications, such as filtration, fuel cells, and molecular sieving. The findings highlight the potential of PBI-based electrospun membranes as versatile materials, offering high thermal stability, chemical resistance, and tunable properties, thereby establishing a foundation for further innovation in advanced polymeric membrane design and applications for energy and sustainability. Full article

The increasing demand for sustainable materials has renewed interest in recycling polyolefins, particularly polypropylene (PP), due to its widespread use and environmental persistence. Post-consumer recycled polypropylene (PP_r), however, often exhibits compromised properties from prior exposure to thermal, oxidative, and mechanical degradation. This study investigates the potential of using post-consumer PP_r in melt-blended extrusion formulations with virgin PP (PP_v), focusing on how different PP_r contents affect processability, thermal stability, oxidative resistance, and mechanical performance. Blends containing 25%, 50%, and 75% PP_r, as well as 100% PP_r and virgin PP, were evaluated using melt flow index (MFI), differential scanning calorimetry (DSC), oxidation induction time (OIT), thermogravimetric analysis (TGA), and tensile testing. Results show that increasing PP_r content improves polymer fluidity and thermal stability under inert conditions but significantly reduces oxidation resistance and ductility. However, the 25% PP_r blend demonstrated a favourable balance between performance and recyclability, presenting 96% of the elastic modulus and 101% of the yield strength of PP_v. Homogenization by extrusion improved the oxidative stability of recycled PP by 22% compared to its non-extruded form. These findings support the use of low-to-moderate levels of PP_r in virgin PP for applications requiring predictable and tunable performance. contributing to circular economy goals. Full article

Background/Objectives: Cirsium setosum (commonly known as thistle) is a traditional Chinese medicinal plant with significant therapeutic potential, exhibiting hemostatic, antioxidant, and wound-healing properties. Electrospinning offers a versatile platform for fabricating nanoscale scaffolds with tunable functionality, making them ideal for drug delivery and tissue engineering. Methods: In this study, a bioactive extract from thistle was obtained and incorporated into a thermosensitive triblock copolymer (PNNS) and polycaprolactone (PCL) to develop a multifunctional nanofibrous scaffold for enhanced wound healing. The prepared nanofibers were thoroughly characterized using Fourier-transform infrared spectroscopy (FTIR), contact angle measurements, thermogravimetric analysis (TGA), and tensile fracture testing to assess their physicochemical properties. Results: Notably, the inclusion of PNNS imparted temperature-responsive behavior to the scaffold, enabling controlled deformation in response to thermal stimuli—a feature that may facilitate wound contraction and improve scar remodeling. Specifically, the scaffold demonstrated rapid shrinkage at a physiological temperature (38 °C) within minutes while maintaining structural integrity at ambient conditions (20 °C). In vitro studies confirmed the thistle extract’s potent antioxidant activity, while in vivo experiments revealed their effective hemostatic performance in a liver bleeding model when delivered via the composite nanofibers. Thistle extract and skin temperature-responsive contraction reduced the inflammatory outbreak at the wound site and promoted collagen deposition, resulting in an ideal wound-healing rate of above 95% within 14 days. Conclusions: The integrated strategy that combines mechanical signals, natural extracts, and electrospinning nanotechnology offers a feasible design approach and significant technological advantages with enhanced therapeutic efficacy. Full article

This study explores the biosynthesis, characterization, and evaluation of silver nanoparticles coated with chitosan (AgChNPs) for liquid nanocomposite and biofilm formation in integrated pest management (IPM). AgChNPs were synthesized using Galega officinalis leaf extract as a reducing agent, with varying chitosan concentrations (0.5%, 1%, and 2%) and pH levels (3, 4, and 5). Synthesis was optimized based on nanoparticle size, stability, and polydispersity index (PDI) over 21 days. Biofilms incorporating AgChNPs were analyzed for chemical, physical, mechanical, and thermal properties via Ultraviolet-visible spectroscopy (UV-vis), Dynamic Light Scattering (DLS), Zeta Potential Analysis, Fourier Transform Infrared Spectroscopy (FTIR), X-Ray Diffraction (XRD), Transmission Electron Microscopy with Energy Dispersive X-ray Spectroscopy (TEM-EDX), and Inductively Coupled Plasma Optical Emission Spectroscopy (ICP-OES) to quantify silver ionization. TEM confirmed spherical nanoparticles (5.54–61.46 nm), and FTIR validated G. officinalis functionalization on chitosan. AgChNPs with 1% chitosan at pH 4 exhibited optimal properties: a size of 207.88 nm, a zeta potential of +42.30 mV, and a PDI of 0.62. Biofilms displayed tunable mechanical strength, with a tensile strength of 3.48 MPa using 5% glycerol and 2% chitosan and an elongation at break of 24.99 mm. TGA showed a two-step degradation process (98.19% mass loss). Ag ionization was 62.57 mg/L in the liquid nanocomposite and 184.07 mg/kg in the biofilms. These findings highlight AgChNPs’ potential for controlled-release properties and enhanced mechanical performance, supporting sustainable agricultural applications. Full article

Cis-1,4-polyisoprene is a widely used elastomer that demonstrates particular thermal and mechanical characteristics, in which the latter is influenced by temperature and strain rate. Molecular dynamic simulations were used to obtain thermal conductivities, glass transition temperatures (T_g), and tensile deformation. Thermal conductivities were calculated by applying the Green–Kubo method, and a decrease in thermal conductivity was observed with increasing temperature. Density–temperature relations were used to calculate T_g, which indicates the transition from the glassy to the rubbery state of the material, and this temperature influences mechanical properties. Investigation of the mechanical properties under uniaxial tensile deformation for constant strain rates indicates an increase in the stiffness and strength of the material at lower temperatures, while increasing molecular mobility at higher temperatures results in reducing these properties. The influence of strain rates at constant temperature highlighted the viscoelastic nature of the structure; increasing strain rates resulted in increases in stiffness, strength, elongation at maximum strength, and elongation at break because of restricted molecular relaxation time. The united-atom force field contributes to higher computational efficiency, which is suitable for large-scale simulations. These results provide important information on the thermo-mechanical properties and tunability of cis-1,4-polyisoprene, which supports applications in the production of interactive fiber rubber composites. Full article

Flexible, biocompatible, and adhesive materials are vital for wearable strain sensors in bioelectronics. This study presents zein-polyaniline (ZPANI) hydrogels with mechanoresponsive energy-harvesting properties. SEM revealed a sheet-like fibrous morphology, enhancing adhesion. Incorporating 0.5 wt% polyaniline (PANI) introduced nanostructured aggregates, while higher PANI concentrations (3–5 wt%) formed intertwined fibrous networks, improving the mechanical integrity, surface area, and conductivity. PANI enhanced electrical conductivity, and the hydrogels displayed excellent swelling behavior, ensuring flexibility and strong tissue adhesion. Biocompatibility was validated through fibroblast cell culture assays, and the adhesive properties were tested on substrates, such as porcine skin, steel, and aluminum, demonstrating versatile adhesion. The adhesion strength of hydrogels to porcine skin was greatly enhanced with an increasing amount of PANI. The maximum adhesion strength was found to be 30.1 ± 2.1 kPa for ZPANI-5.0. Mechanical testing showed a trade-off between strength and conductivity. The tensile strength decreased from 13.4 kPa (ZPANI-0) to 7.1 kPa (ZPANI-5.0), and the compressive strength declined from 18.5 kPa to 1.6 kPa, indicating increased brittleness. A rheological analysis revealed enhanced strain tolerance (>500% strain) with an increasing PANI content. The storage modulus (G′) remained stable up to 100% strain in PANI-free hydrogels but collapsed beyond 450% strain, while PANI-containing hydrogels exhibited improved viscoelasticity. Mechanical testing showed robust voltage output signals under compression within a 20 s response time. Despite the reduced mechanical strength, energy-harvesting tests showed a surface power density of 0.12 nW cm⁻², charge storage of 0.71 nJ, and a surface energy density of 1.4 pWh cm⁻². The synergy of the piezoelectric response, bioadhesion, and tunable viscoelasticity establishes ZPANI hydrogels as promising candidates for wearable sensors and energy-harvesting applications. Optimizing the PANI content is crucial for balancing mechanical stability, adhesion, and electrical performance, ensuring long-term bioelectronic functionality. Full article

The catalytic performance of α-diiminonickel complexes is highly sensitive to structural modifications in their ligand frameworks. In this study, a series of unsymmetrical 2,3-bis(arylimino)butane-nickel complexes featuring ortho-2,6-dibenzhydryl groups as sterically demanding motifs and para-methyl groups as electron-donating enhancers were proposed and synthesized. These nickel complexes were thoroughly characterized using FTIR, elemental analysis, and single-crystal X-ray diffraction (for Ni4 and Ni5), revealing deviations from ideal tetrahedral geometry. Upon activation with Et₂AlCl, these complexes demonstrated exceptional ethylene polymerization activity, achieving a remarkable value of 13.67 × 10⁶ g PE mol⁻¹ (Ni) h⁻¹ at 20 °C. Notably, even at 80 °C, the nickel complexes maintained a high activity of 1.97 × 10⁶ g PE mol⁻¹ (Ni) h⁻¹, showcasing superiority compared to previously reported unsymmetrical 2,3-bis(arylimino)butane-nickel complexes. The resulting polyethylenes exhibited ultra-high molecular weights (M_w: 3.33–19.47 × 10⁵ g mol⁻¹) and tunable branching densities (84–217/1000C), which were effectively controlled by polymerization temperature. Moreover, the mechanical properties of the polyethylenes, including tensile strength (σ_b = 0.74–16.83 MPa), elongation at break (ε_b = 271–475%), and elastic recovery (SR = 42–74%), were finely tailored by optimizing molecular weight, crystallinity, and branching degree. The prepared polyethylenes displayed outstanding elastic recovery, a hallmark of high-performance thermoplastic elastomers, making them promising candidates for advanced material applications. Full article

The development of biodegradable alternatives to petroleum-based packaging is essential for environmental sustainability. This study presents a novel approach to enhance the performance of hemicellulose-based films by fabricating xylan/polyvinyl alcohol (PVA) composites reinforced with zinc oxide nanoparticles (nano-ZnO). To address nano-ZnO agglomeration, sodium hexametaphosphate (SHMP) was utilized as a dispersant, while sorbitol improved film flexibility. The composite films were prepared via solution casting, and the effects of nano-ZnO content (0–2.5 wt%) on mechanical, thermal, and barrier properties were systematically evaluated. Results showed that at 2 wt% nano-ZnO loading, the tensile strength increased from 15.0 MPa (control) to 26.15 MPa, representing a 74% enhancement, while oxygen permeability decreased from 1.83 to 0.50 (cm³·μm)/(m²·d·kPa). Additionally, the thermal stability also improved due to hydrogen bonding and uniform nanoparticle dispersion. At this optimized loading, the hydrophobcity was also maximized, with the contact angle peaking at 74.4° and water vapor permeability decreasing by 18% (1.53·10⁻⁶·g·h⁻¹·m⁻¹·Pa⁻¹). Excessive nano-ZnO loading (>2 wt%) induced particle agglomeration, generating stress concentrators that disrupted the polymer–nanoparticle interface and compromised mechanical integrity. These findings highlight the potential of nano-ZnO-modified xylan/PVA films as sustainable, high-performance alternatives to conventional packaging. The synergistic use of SHMP and nano-ZnO provides a strategy for designing eco-friendly materials with tunable properties, advancing the use of biomass in food preservation applications. Full article

The development of sustainable and mechanically versatile polymeric materials is essential to meet the growing demand for eco-friendly, high-performance products. This study investigates the mechanical properties of blends comprising polyvinyl chloride (PVC), thermoplastic polyurethane (TPU), and glycerol diacetate monolaurate, a bio-based plasticizer derived from waste cooking oil, addressing the underexplored combined effects of these components. By varying the proportions, the blends’ tensile strength, elasticity, elongation at break, and hardness were tailored for diverse applications. Incorporating the bio-plasticizer significantly enhanced the PVC’s flexibility and elongation at break, while reducing its tensile strength and rigidity. The addition of TPU further enhanced the elasticity, toughness, and resilience, with the final properties governed by synergistic interactions between PVC’s rigidity, TPU’s elasticity, and the plasticizer’s softening effects. Dynamic mechanical analysis (DMA) confirmed that the bio-plasticizer enhanced the compatibility between the PVC and TPU, leading to ternary PVC/TPU/bio-plasticizer blends with an improved elasticity and elongation at break, without a significant loss in tensile strength. These blends exhibited a broad range of tunable properties, enabling applications from flexible films to impact-resistant components. Overall, these findings highlight the potential of PVC/TPU/bio-plasticizer systems to deliver high-performance materials with enhanced sustainability. This work offers valuable insights for developing greener polymer systems and advancing the creation of tailored materials for diverse industrial applications in alignment with global sustainability goals. Full article