Search Results (2,943)

This study demonstrates a molecular size-dependent strategy to regulate the network structure of poly(vinyl alcohol) (PVA) hydrogels using a series of saccharides with increasing molecular size—glucose, maltose, raffinose, soluble starch, and amylose. FTIR, XPS, XRD, and TG analyses reveal that increasing saccharide size shifts the network from plasticization to reinforcement, which is further confirmed by mechanical testing and rheological analysis. Small-molecule saccharides disrupt hydrogen bonds and enhance chain mobility, while macromolecular starches promote network regularity through strong hydrogen bonding and crystallization induction. This structural tunability ndows the resulting hydrogels with integrated functionalities: tensile strain increases from 640% to 1500%, self-healing efficiency reaches up to 90.6%, and high-fidelity electrocardiogram (ECG) signal acquisition is achieved with a signal-to-noise ratio of 39.84 dB, comparing favorably with commercial electrodes. This work establishes a structure–property relationship linking saccharide molecular size to network architecture and provides a versatile material platform for next-generation flexible wearable sensors and bioelectrodes. Full article

A ligand-free Ni(acac)₂/EASC Ziegler–Natta catalytic system was developed for the efficient synthesis of low molecular weight liquid polybutadiene (LPB) featuring high 1,4 content. The influences of key polymerization parameters, including Al/Ni ratio, polymerization temperature, monomer-to-catalyst ratio ([Bd]/[Ni]), and external donors, were systematically investigated to elucidate structure–reactivity relationships. Increasing the Al/Ni ratio significantly enhances catalytic activity while promoting chain transfer reactions, leading to reduced molecular weights and broader molecular weight distributions, with minimal impact on overall 1,4 selectivity. Polymerization temperature strongly affects both activity and stereoselectivity; elevated temperatures accelerate chain transfer processes and broaden dispersity, while inducing a shift from kinetically favored cis-1,4 insertion toward increased trans-1,4 incorporation. Variation of the [Bd]/[Ni] ratio provides an effective handle for molecular weight regulation, where higher ratios favor chain propagation over chain transfer, affording higher molecular weights but lower monomer conversion. Notably, the system maintains consistently high 1,4 content (>98%) across a wide range of conditions. In contrast, the introduction of external donors markedly affects catalytic behavior depending on their coordination ability. Strongly coordinating O- and S-containing donors partially deactivate the catalyst and significantly shift regioselectivity toward 1,2-vinyl incorporation (up to ~20%), while N- and P-containing donors are well tolerated and can increase molecular weight by suppressing chain transfer pathways, which also results in products with higher 1,2 content. Full article

Cement stabilized macadam (CSM) bases are prone to cracking and void damage under long-term traffic loading and environmental actions, which accelerates structural deterioration. Although grouting is an effective method for treating such concealed defects, laboratory-based evaluation of repair effectiveness remains limited. In this study, field-cored CSM specimens were recombined in a cylindrical mold to simulate four void conditions (1/4, 2/4, 3/4, and 4/4), and repaired using an inorganic cementitious composite grouting material based on ultra-fine cement and high-belite sulphoaluminate cement (HBSAC), and modified with ethylene-vinyl acetate (EVA) latex, wollastonite (WO) whiskers, and polyvinyl alcohol (PVA) fibers. The repair effectiveness was evaluated through ultrasonic testing, capacitance measurement, uniaxial compression with acoustic emission (AE) monitoring, and computed tomography (CT). The results show that the longitudinal wave velocity of all repaired groups increases continuously with curing time, with a maximum increase of 21.98% at 28 days. The normalized capacitance response exhibits clear time- and layer-dependent variation, with the 4/4 group showing the most pronounced spatial heterogeneity. In the uniaxial compression tests, the peak load increases from 181 kN in the control group to 201–286 kN in the repaired groups, while the tensile-related AE event proportion increases from 77.35% in the 1/4 group to 89.38% in the 4/4 group. CT analysis shows that the proportion of micropores smaller than 1 mm³ increases from 66.3% to 82.7%, whereas the proportion of pores larger than 100 mm³ decreases from 46.5% to 21.6% after repair. These results demonstrate that the composite grouting material provides effective filling, structural reconstruction, and mechanical enhancement for void-damaged CSM, and that the proposed multi-source characterization framework is suitable for evaluating grouting repair performance. Full article

This study examined how the extraction medium used to obtain Quercus robur extracts influenced the properties of electrospun poly(vinyl alcohol) (PVA) mats intended for potential active packaging applications. Extracts prepared with 50% ethanol and with a choline chloride:lactic acid:water system were incorporated into PVA spinning solutions, and their effects on solution properties, fiber morphology, thermal behavior, crosslinking response, and polyphenol release were evaluated. The type of extraction medium affected both the electrospinning process and the structure of the resulting materials. Ethanol-derived extracts reduced solution viscosity and promoted the formation of thinner fibers, whereas systems containing the choline chloride:lactic acid:water-derived extract showed higher conductivity and lower electrospinning stability. Crosslinking with tannic acid in water led to the collapse of the fibrous structure, while ethanolic tannic acid treatment preserved the nanofibrous morphology more effectively. FTIR analysis indicated differences in intermolecular interactions within the polymer matrix, consistent with the observed changes in structural stability and release behavior. Thermal analysis showed that ethanol-derived extracts lowered the thermal stability of the PVA matrix, whereas the choline chloride:lactic acid:water-derived system altered the degradation pathway and increased the amount of solid residue formed during heating. Release studies demonstrated a rapid burst release for ethanol-based mats and a more sustained release profile for mats containing the choline chloride:lactic acid:water-derived extract. Selected extract-containing and ethanol–tannic acid-crosslinked mats also showed antibacterial activity against Staphylococcus aureus. The results showed that the extraction medium significantly affected polymer–extract interactions and the functional properties of electrospun PVA mats. At the same time, the conclusions refer specifically to the tested solvent systems, and broader generalization to other natural deep eutectic solvent-type formulations requires further comparative studies. Full article

In the process of extracting and transporting waxy crude oil, pipeline blockages resulting from wax deposition significantly impede production efficiency and lead to substantial economic losses. Ethylene vinyl acetate copolymer (EVA) is a widely used chemical wax inhibitor; however, its performance is influenced by multiple factors, including its molecular structure, concentration, and the carbon number distribution of the wax system. A systematic elucidation of its mechanism of action and associated phase changes is therefore necessary. In this study, differential scanning calorimetry (DSC) was employed to systematically investigate the thermal behavior of a wax system with a broad carbon number distribution (C5–C50). The objectives were to analyze the influence of EVA concentration, vinyl acetate (VA) content, and molecular weight on the phase transition parameters, to elucidate the wax inhibition mechanism, and to construct a phase prediction model based on the Flory–Huggins theory. The results demonstrate that the wax appearance temperature (WAT), phase transition temperature, and phase transition enthalpy of the wax systems increase monotonically with carbon number. Furthermore, the addition of EVA was found to significantly reduce both the WAT and the amount of wax precipitated. The optimal structural parameters were identified as a VA content of 10%, a number average molecular weight of 20,000, and an optimal concentration of 800 ppm. The medium-carbon wax system (C16–C30) was found to be the most sensitive to the EVA response. The established phase model exhibited high predictive accuracy, with a mean relative error of less than 4%, a root mean square error (RMSE) of 0.32%, and a coefficient of determination (R²) of 0.987, thereby providing preliminary insights and a practical tool for optimizing EVA wax inhibitor formulations under simplified conditions and guiding their potential engineering applications. Full article

Volatile organic compounds (VOCs) are ubiquitous pollutants, and exposure from in utero through childhood may impair neurodevelopment. However, compound-specific risks remain unclear. This systematic review and meta-analysis examined associations between VOC exposure and child neurodevelopmental outcomes. A systematic search of PubMed, Scopus, and Embase was conducted until August 2025, yielding 1213 records. Quality assessment was performed using the Newcastle–Ottawa Scale and risk of bias using the ROBINS-E tool. Pooled odds ratios (ORs) were calculated using random-effects models, with heterogeneity evaluated via I² statistics. Subgroup analyses explored for study design, exposure timing, and country income level. Twenty-eight studies were included in the final analysis. Of the 18 VOCs analyzed, five compounds, propionaldehyde (pooled OR = 1.84; 95% CI 1.19–2.49), styrene (pooled OR = 1.69; 95% CI 1.30–2.21), vinyl chloride (pooled OR = 1.53; 95% CI 1.24–1.89), acrolein (pooled OR = 1.48; 95% CI 1.08–2.04), and trichloroethylene (OR = 1.21; 95% CI 1.04–1.41), demonstrated statistically significant adverse associations with neurodevelopment. Benzene showed borderline significance. Heterogeneity ranged from 0–47%. Subgroup analyses identified significant effect modification for 1,3-butadiene by study design and exposure timing and higher pooled estimates for ethylbenzene in high-income countries. Full article

The development of sustainable encapsulation materials with tunable thermomechanical properties remains a critical challenge for photovoltaic reliability. Currently, the mainstream encapsulant for polycrystalline silicon solar cells is crosslinked EVA (Ethylene-Vinyl Acetate), which complicates the end-of-life recycling and reuse of modules. There is an urgent need to develop a novel encapsulant that combines excellent barrier properties with thermoplastic recyclability. Herein, we report a novel series of thermally decomposable CO₂-based thermoplastic polyurethane (PPC-TE) films engineered through the rational design of soft and hard segments. Utilizing polycarbonate diol (PPCDL) and polyether glycol (PEG) as soft segments, we systematically tailor material properties by modulating PEG-to-PPCDL ratios (5–20 wt%) and PEG molecular weights (1000–4000 g/mol). The optimized PPC-TE films exhibit excellent transmittance (>90%), adjustable glass transition temperature (T_g: 35.1 °C~11.6 °C), and remarkable mechanical adaptability (51~92 HA). The PPC-TE films exhibit water vapor permeability (WVP) as low as 14.8 g·mm·m⁻²·day⁻¹ and oxygen permeability (OP) of 4.13 cc·mm·m⁻² day⁻¹ at 15 wt% PEG content, surpassing commercial ethylene–vinyl acetate (EVA) encapsulants. Notably, these films demonstrate fully thermal decomposition above 350 °C, facilitating eco-friendly photovoltaic device recycling. Superior adhesion to glass substrates is evidenced by peel strengths up to 37 N/cm (PPC-TE2000-20) and the shrinkage rate is as low as 3%. This work contributes to improving the long-term stability of solar cells and has the potential for large-scale production. Full article

Over the past decades, plastics have been increasingly employed to package foods and beverages. Furthermore, foods, nowadays, are kept in contact with plastics for far longer periods than ever before. A number of conventional polymers, i.e., polyethylene (PE), Polypropylene (PP), Ethylene Vinyl Acetate (EVA), Εthylene vinyl alcohol (EVOH) polystyrene (PS), Polyvinyl chloride (PVC), Polyvinylidene chloride (PVDC), polyethylene terephthalate (PET), Polycarbonate (PC), polyethylene naphthalate (PEN), Polyamides (PAs), Polyacrylonitrile (PAN) as well as biodegradable polymers-[Polylactide (PLA)] are used commercially in food packaging applications. Potential interaction of food with the packaging container includes: permeation, migration and flavor scalping. Most food and beverage containers are lined with plastics mainly polyolefins, which due to their low polarity tend to absorb volatile compounds of similar polarity. Absorption of flavor compounds by polymers involves both partitioning and diffusion through the plastic. Absorption is influenced by (i) polymer properties such as polarity, morphology, glass transition temperature, density, free volume, crystallinity and surface area, (ii) flavor compound properties such as structure, concentration, and polarity, and (iii) external factors such as temperature, time of contact, relative humidity and the proximity of other compounds. Based on the above, it is apparent that flavor scalping should be among one of the food packaging industry priorities in order to efficiently preserve the quality of packaged food flavor. This review highlights the various factors affecting the scalping process, as well as the consequences of flavor scalping in various food and beverage commodities. The review covers the period 1990–2925 and used the LitChemPlast data base for literature search. Full article

Flexible and wearable electronics require soft sensing materials that balance mechanical compliance, stable signal transduction, and durability for human–machine interfaces (HMIs). To address the limitations of single-filler systems, we propose a poly(vinyl alcohol) (PVA)/aramid nanofiber (ANF)/MXene organogel (PAM) as a multifunctional soft platform. This design integrates a PVA physically crosslinked network with ANF for mechanical reinforcement and MXene for electrical functionality. The optimized PAM composite exhibits outstanding mechanical properties, including a fracture stress of 2931 kPa, a fracture strain of 676%, and a fracture toughness of 9.04 MJ m⁻³. Importantly, PAM serves as a single material platform configurable into three sensing modalities. The resistive strain sensor achieves a gauge factor of 3.1 over 10–100% strain and enables the reliable recognition of human joint movements and gestures. The capacitive pressure sensor delivers a sensitivity of 0.298 kPa⁻¹, rapid response/recovery times of 30/10 ms, and is integrated with a wireless module to control a smart car. Furthermore, the PAM-based triboelectric nanogenerator (TENG) delivers excellent electrical outputs (V_oc = 123 V, I_sc = 0.52 μA, Q_sc = 58 nC) and functions as a self-powered smart handwriting pad, achieving a machine-learning-based recognition accuracy of 97.6%. This work demonstrates the immense potential of the PAM organogel for advanced, self-powered HMIs. Full article

To achieve the same service life of glass fiber reinforced polymer (GFRP) connectors and precast concrete sandwich panels, ensuring the structural stability and safety of the walls during long-term service, it is necessary to research the durability of GFRP connectors. In accordance with the ACI 440.3R-12 test method, an accelerated aging study was conducted by immersing 90 GFRP connectors in a simulated concrete pore solution at temperatures of 40 °C, 60 °C, and 80 °C for durations of 3.65, 18, 36.5, 92, and 183 days. This investigation aimed to analyze the effects of temperature and exposure time on the shear strength of the GFRP connectors. Scanning Electron Microscopy (SEM) was employed to analyze the micro-morphology of the specimens before and after exposure. The SEM observations revealed that after 183 days at 40 °C, the fiber-matrix interface remained relatively intact without significant debonding. However, at 60 °C, noticeable degradation occurred, characterized by corrosion of fibers and evident debonding from the surrounding matrix. At 80 °C, the GFRP specimens were severely damaged, precluding the extraction of viable samples for SEM analysis. The results further indicated that the most rapid decline in the shear strength occurred within the initial 3.65 days of exposure, with reductions of 8.62%, 10.12%, and 10.77% at 40 °C, 60 °C, and 80 °C, respectively. The degradation rate subsequently decelerated with prolonged exposure. After 183 days, the residual shear strength retention rates decreased by 21.03% and 26.89% at 40 °C and 60 °C, respectively. This behavior is primarily attributed to a high moisture absorption rate driven by a significant humidity gradient between the surface and the interior, leading to rapid swelling and plasticization of the vinyl ester resin matrix, which consequently reduced the stiffness and strength of the GFRP connectors. Finally, a predictive model for the time-dependent shear strength of GFRP connectors under various temperature conditions was developed based on Fick’s law. Full article

Lignin is an abundant aromatic biopolymer, but its conversion into high-performance fibers remains challenging due to intrinsically poor spinnability, structural heterogeneity, and inefficient stress transfer in lignin-rich systems. In this study, a processing and structure strategy is demonstrated to overcome these limitations by transforming industrial black-liquor kraft lignin into a spinnable and load-bearing fiber component. Kraft lignin recovered from black-liquor waste was extracted and subsequently purified using a hot-water treatment to remove inorganic impurities and thermally unstable fractions, increasing lignin purity to 95.9% through extensive deionized water purification using a water-to-lignin ratio of 300:1. The purified lignin was then blended with poly(vinyl alcohol) (PVA), wet-spun into continuous filaments, and subjected to post-spinning hot drawing to induce molecular orientation. This sequential extraction, purification, blending, spinning, and drawing approach enables stable wet spinning and the continuous formation of lignin-rich lignin/PVA filaments without filament breakage, directly addressing the primary processing bottleneck of lignin-based fibers. Molecular-level miscibility between lignin and PVA is confirmed by the presence of a single glass transition temperature at 88.3 °C, indicating the formation of a homogeneous amorphous phase. SEM observations reveal composition-dependent surface roughness and non-circular cross-sectional morphologies arising from differential coagulation and shrinkage, demonstrating that lignin actively participates in the load-bearing fiber network rather than acting as a passive filler. As a result of purification-enabled spinnability, true blend miscibility, and post-spinning hot drawing, fibers with a lignin-to-PVA composition of 40:60 achieve a maximum tensile strength of 2.8 GPa, approaching the performance range of commercial high-strength polymer fibers. This work establishes a clear relationship between material structure, processing strategy, and resulting properties, highlighting the potential of industrial lignin waste as a sustainable precursor for advanced fiber applications. Full article

Poly(vinyl alcohol)/chitosan (PVA/CS) biodegradable films reinforced with acid-functionalized multi-walled carbon nanotubes (f-MWCNTs) were fabricated via solution casting to investigate the effects of nanotube incorporation on structural, mechanical, thermal, dielectric, and physicochemical properties. Unlike conventional CNT-reinforced systems, this study focuses on the role of acid functionalization in improving nanotube dispersion and interfacial interactions, enabling simultaneous enhancement of multiple performance characteristics. Fourier transform infrared spectroscopy (FTIR) analysis confirmed strong intermolecular interactions between PVA/CS functional groups and carboxyl groups on f-MWCNTs, while scanning electron microscopy (SEM) revealed homogeneous nanotube dispersion at low loadings and partial aggregation at higher contents. X-ray diffraction (XRD) indicated that crystallinity was modified in a non-monotonic manner with increasing nanotube concentration due to competing nucleation and chain-restriction effects, while dielectric measurements showed an increase in dielectric constant from 3.78 to 4.27 as a result of enhanced interfacial polarization. The thermal conductivity improved from 0.195 to 0.247 W·m⁻¹·K⁻¹, and tensile strength increased from 19.8 to 24.5 MPa at 0.2 wt.% f-MWCNT, with elongation at break decreasing from 37.9% to 25.1%, reflecting increased stiffness. The degree of swelling and water solubility decreased with higher nanotube content, indicating reduced hydrophilicity and enhanced structural compactness. The results provide new insights into how surface-functionalized nanofillers can be used to tailor the multifunctional performance of biodegradable polymer nanocomposite films, highlighting their potential in advanced applications such as sustainable packaging, flexible electronics, sensors, and membrane technologies. Full article

Type 2 endoleaks (EL2s) are potentially life-threatening complications, defined as persistent arterial perfusion of the excluded aneurysmal sac after endovascular aneurysm repair (EVAR). Most EL2s are managed endovascularly, through embolization of the aneurysmal sac and its arterial feeders. During embolization, attention should be given to anatomical variants such as “corona mortis”, an arterial anastomosis connecting external iliac (via inferior epigastric) and internal iliac (via obturator) arteries. We present the case of an 88-year-old male previously treated with EVAR for a left common iliac artery aneurysm (CIAA), complicated by EL2 originating from the ipsilateral ilio-lumbar branch of the internal iliac artery. Successful embolization of the endoleak was achieved through catheterization of the inferior epigastric artery, taking advantage of the “corona mortis” variant. This route allowed access to the sac and embolization with ethylene-vinyl-alcohol-copolymer. This approach represents a safe alternative to direct sac puncture or superior gluteal artery access in patients exhibiting this anatomical variant. Full article

In the pursuit of sustainable and flexible electronics, polymer-based conductive films offer a promising solution due to their biodegradability, mechanical flexibility, and cost-effective fabrication. This study presents the development of a highly conductive and flexible nanocomposite material based on polyaniline-grafted chitosan (PANI-g-Chs) and Vinavil (Vi, a vinyl glue specifically designed for enhancing the sealability of textiles and paper), serving as a matrix for applications in flexible electronics. The PANI-g-Chs nanocomposite was synthesized via in situ oxidative polymerization, where chitosan nanoparticles (Chs) served as a stabilizing template to prevent PANI aggregation, reducing the particle size from 1700 nm (pristine PANI) to 180 nm (PANI-g-Chs). The resulting composite exhibited exceptional electrical conductivity (77.79 S/m at 25 wt% PANI-g-Chs). Hall effect measurements showed that the carrier mobility increased up to 1162.7 cm²/V·s and the carrier density rose to 6.5.1017 cm⁻³, confirming efficient charge transport and network formation. Mechanical analysis revealed a 300% increase in the storage modulus for PANI-g-Chs, and thermal studies confirmed stability up to 300 °C. Optical characterization showed a reduced bandgap (3.6 eV) and extended π-conjugation, which are critical for optoelectronic applications. Application tests demonstrated stable conductivity under mechanical deformation, highlighting the material’s potential for use in flexible electronics, sensors, and sustainable conductive coatings. This work offers a viable alternative to conventional conductive polymers. Full article

Gypsum-based materials are widely used in construction but suffer from poor water resistance and durability, limiting their application in moisture-prone environments. While fiber-reinforced modified gypsum (FRMG) improves mechanical performance, the lack of systematic research on waterproofing strategies and their influence on both durability and strength remains a key challenge. This study investigated three waterproofing methods: surface coating with paraffin emulsion, internal incorporation of paraffin emulsion, and internal incorporation of vinyl acetate ethylene (VAE) emulsion. The workability, water absorption, mechanical properties, contact angle, and microstructure of the FRMG matrix were analyzed. The results showed that surface coating provided only short-term waterproofing. Internal incorporation of paraffin emulsion reduced water absorption but weakened mechanical performance. In contrast, VAE emulsion formed continuous polymer films that filled pores, significantly reducing water absorption while improving flexural and compressive strength, with optimal performance observed at a 6% dosage. In addition, increasing emulsion content enhanced hydrophobicity. These results indicate that VAE-based internal modification is an effective approach to improving the durability and performance of gypsum-based materials, providing guidance for their application in interior wall systems and prefabricated building components. Full article