Search Results (733)

This study analyzes the thermal degradation of PVA and PVA/glycerol films in air under varying heating rates. Thermogravimetric analysis (TGA) of pure PVA in both air and inert atmospheres confirmed that oxidative conditions significantly influence degradation, particularly at lower heating rates. For PVA/glycerol films in air, deconvolution of the differential thermogravimetry (DTG) curves during the main degradation stage revealed distinct peaks attributable to the degradation of glycerol, PVA/glycerol complexes, and PVA itself. Isoconversional methods showed that, for pure PVA in air, the apparent activation energy (Ea) increased with conversion, suggesting the simultaneous occurrence of multiple degradation mechanisms, including oxidative reactions, whose contribution changes over the course of the degradation process. In contrast, under an inert atmosphere, Ea remained nearly constant, consistent with degradation proceeding through a single dominant mechanism, or through multiple steps with similar kinetic parameters. For glycerol-plasticized films in air, Ea exhibited reduced dependence on conversion compared with that of pure PVA in air, with values similar to those of pure PVA under inert conditions. These results indicate that glycerol influences the oxidative degradation pathways in PVA films. These findings are relevant to high-temperature processing of PVA-based materials and to the design of thermal treatments—such as sterilization or pyrolysis—where control over degradation mechanisms is essential. Full article

This study involved the fabrication of poly (vinyl alcohol) (PVA) nanocomposite films using the solution-casting process, which incorporated strontium-coated silver oxide (Sr-Ag₂O) nanoparticles generated by a plant-extract assisted method. Various characterization techniques, such as XRD, SEM, TEM, UV, and FTIR, showed the formation and uniform distribution of Sr-Ag₂O nanoparticles in the PVA film, which are biocompatible nanocomposite films. The presence of hydroxyl groups leads to appreciable mixing and interaction between the Sr-Ag₂O nanoparticles and the PVA polymer. Mechanical and thermal results suggest enhanced tensile strength and increased thermal stability. In addition, the sample of PVA/Sr-Ag₂O (1.94/0.06 wt. ratio) nanocomposite film showed decreased hydrophilicity, lower hemolysis, non-toxicity, and appreciable cell migration activity, with nearly 19.95% cell migration compared to the standard drug, and the presence of Sr-Ag₂O nanoparticles favored the adhesion and spreading of cells, which triggered the reduction in the gaps. These research findings suggest that PVA/Sr-Ag₂O nanocomposite films with good mechanical, antimicrobial, non-toxic, and biocompatible properties could be applied in biological wound-healing applications. Full article

Achieving carbon neutrality requires not only reducing CO₂ emissions but also capturing atmospheric CO₂. Direct air capture (DAC) using amine-based adsorbents has emerged as a promising approach. In this study, we developed amine-epoxy/poly(vinyl alcohol) (AE/PVA) nanofibers via electrospinning and in situ thermal polymerization. PVA was incorporated to enhance spinnability, and B-staging of AE enabled fiber formation without inline heating. We systematically investigated the effects of electrospinning parameters, epoxy-to-amine ratios (E/A), and the degree of PVA saponification on CO₂ adsorption performance. Thinner fibers, obtained by adjusting spinning conditions, exhibited faster adsorption kinetics due to increased surface area. Varying the E/A revealed a trade-off between adsorption capacity and low-temperature desorption efficiency, with secondary amines offering a balanced performance. Additionally, highly saponified PVA improved thermal durability by minimizing side reactions with amines. These findings highlight the importance of optimizing fiber morphology, chemical composition, and polymer properties to enhance the performance and stability of AE/PVA nanofibers for DAC applications. Full article

Bio-nanocomposites based on poly (vinyl alcohol) (PVA) and cellulosic nanostructures are favorable for active food packaging applications. The current study systematically investigates the mechanical properties, gas permeation, and swelling parameters of PVA composites with cellulose nanocrystals (CNC) or nano lignocellulose (NLC) fibers. Alterations in these macroscopic properties, which are critical for food packaging applications, are correlated with structural information at the molecular level. Strong interactions between the fillers and polymer host matrix were observed, while the PVA crystallinity exhibited a maximum at ~1% loading. Finally, the orientation of the PVA nanocrystals in the uniaxially stretched samples was found to depend non-monotonically on the CNC loading and draw ratio. Concerning the macroscopic properties of the composites, the swelling properties were reduced for the D1 food simulant, while for water, a considerable decrease was observed only when high NLC loadings were involved. Furthermore, although the water vapor transmission rates are roughly similar for all samples, the CO₂, N₂, and O₂ gas permeabilities are low, exhibiting further decrease in the 1% and 1–5% loading for CNC and NLC composites, respectively. The mechanical properties were considerably altered as a consequence of the good dispersion of the filler, increased crystallinity of the polymer matrix, and morphology of the filler. Thus, up to ~50%/~170% enhancement of the Young’s modulus and up to ~20%/~50% enhancement of the tensile strength are observed for the CNC/NLC composites. Interestingly, the elongation at break is also increased by ~20% for CNC composites, while it is reduced by ~40% for the NLC composites, signifying the favorable/unfavorable interactions of cellulose/lignin with the matrix. Full article

We investigated the practical adhesion of a conventional poly(vinyl alcohol) glue with a glassy isosorbide-based polycarbonate (ISB-PC) comprising isosorbide and 1,4-cyclohexanedimethanol. The addition of 1 wt.% of a copolymer of vinyl alcohol and butenediol to the ISB-PC greatly improved its lap-shear strength. This improvement may be attributed to the dissolution of the copolymer chains in the ISB-PC, which had a low water droplet contact angle. Furthermore, the blend was transparent because most of the copolymer chains dissolved in the ISB-PC. Microplastics present a serious environmental issue, even for adhesives. Therefore, the present technique to modify ISB-PC to show good lap-shear strength with a biodegradable glue is attractive. Full article

The persistent contamination of aquatic environments by heavy metals, particularly Pb²⁺, Cd²⁺, and Cu^2+, poses a serious global threat due to their toxicity, persistence, and bioaccumulative behavior. In response, low-cost and eco-friendly adsorbents are being explored, among which CaCO₃-based biocomposites derived from mollusk shells have shown exceptional performance. In this study, a hybrid biocomposite composed of poly(vinyl alcohol) (PVA) and oyster shell-derived CaCO₃ was computationally investigated using Density Functional Theory (DFT) to elucidate the electronic and structural basis for its high metal-removal efficiency. Calculations were performed at the B3LYP/6-311++G(d,p), M05-2X/6-311+G(d,p), and M06-2X/6-311++G(d,p) levels using GAUSSIAN 16. Among them, B3LYP was identified as the most balanced in terms of accuracy and computational cost. The hybridization with CaCO₃ reduced the HOMO-LUMO gap by 20% and doubled the dipole moment (7.65 Debye), increasing the composite’s polarity and reactivity. Upon chelation with metal ions, the gap further dropped to as low as 0.029 eV (Cd²⁺), while the dipole moment rose to 17.06 Debye (Pb²⁺), signaling enhanced charge separation and stronger electrostatic interactions. Electrostatic potential maps revealed high nucleophilicity at carbonate oxygens and reinforced electrophilic fields around the hydrated metal centers, correlating with the affinity trend Cu²⁺ > Cd²⁺ > Pb²⁺. Fukui function analysis indicated a redistribution of reactive sites, with carbonate oxygens acting as ambiphilic centers suitable for multidentate coordination. Natural Bond Orbital (NBO) analysis confirmed the presence of highly nucleophilic lone pairs and weakened bonding orbitals, enabling flexible adsorption dynamics. Furthermore, NCI/RDG analysis highlighted attractive noncovalent interactions with Cu²⁺ and Pb²⁺, while FT-IR simulations demonstrated the formation of hydrogen bonding (O–H···O=C) and Ca²⁺···O coordination bridges between phases. Full article

Intrinsic conductive ionic hydrogels, endowed with excellent mechanical properties, hold significant promise for applications in wearable and implantable electronics. However, the complexity of exercise and athletics calls for mechanical tunability, facile processability and high conductivity of wearable sensors, which remains a persistent challenge. In this study, we developed a mechanically tunable and high ionic conductive hydrogel patch to approach multi-gesture or motion monitoring. Through adjustment of the ratio of amino trimethylene phosphonic acid (ATMP) and poly(vinyl alcohol) (PVA), the composite hydrogel attains tunable mechanical strength (varying from 50 kPa to 730 kPa), remarkable stretchability (reaching up to 1900% strain), high conductivity (measuring 15.43 S/m), and strong linear sensitivity (with a gauge factor of 2.34 within 100% strain). Benefitting with the tunable mechanical sensitivity, the composite hydrogel patch can perform subtle movement monitoring, such as epidermal pulses or pronounced muscle vibrations; meanwhile, it can also recognize and detect major motions, such as hand gestures. The mechanically tunable composite hydrogel contributes a versatile sensing platform for health or athletic monitoring, with wide and sensitive adoptability. Full article

Polyols derived from poly(vinyl alcohol) (PVA) have not been reported before. The hydroxyalkylation of PVA with oxiranes leads to powdered or gum-like products that are not miscible with isocyanates and therefore useless as sources of polyurethane foams. Glycidol and ethylene carbonates were used to dissolve and convert PVA into liquid polyol. The physical properties of the PVA-derived polyol, such as the density, viscosity, and surface tension, were determined. The polyol was then used to obtain rigid polyurethane foams (PUFs). Foaming conditions were optimized, and the apparent density, volume water uptake, dimensional stability, heat conductance coefficient, pore size, thermal resistance, compressive strength, and glass transition temperature of the obtained PUFs were determined. The properties of the obtained PUFs were similar to those of classic rigid PUFs, but the thermal resistance of the former is better. Specifically, PVA-derived PUFs are thermally resistant at temperatures of up to 150 °C. Furthermore, they are ecologically safe; in standard soil conditions, 54.6% or 100% biodegradation of the foams in cube and powder form, respectively, was observed, as measured by BOD after 28 days of storage. Full article

Anion exchange membrane fuel cells (AEMFCs) have garnered significant attention for their potential to advance fuel cell technology. In this study, we developed and characterized anion exchange membranes (AEMs) composed of quaternized poly(vinyl alcohol) (QPVA) electrospun nanofiber mats with poly(acrylamide-co-diallyldimethylammonium chloride) (PAADDA) as a matrix filler for interfiber voids. The objective was to investigate the effect of varying PAADDA concentrations as a matrix filler for interfiber voids on the structural, mechanical, and electrochemical properties of QPVA-based electrospun AEMs. Membranes with various concentrations of PAADDA were fabricated and extensively characterized using FTIR, SEM, tensile strength, water uptake, swelling degree, ion exchange capacity (IEC), and hydroxide ion conductivity (σ). FTIR confirmed the successful incorporation of PAADDA into the membrane structure, while SEM images showed that PAADDA effectively filled the voids between the QPVA fibers, resulting in denser membranes. The results indicated that the eQPAD5.0 membrane, with the highest PAADDA content, exhibited the best overall performance. The incorporation of PAADDA into QPVA-based electrospun AEMs significantly enhanced their mechanical strength, achieving a tensile strength of 23.9 MPa, an IEC of 1.25 mmol g⁻¹, and hydroxide conductivity of 19.49 mS cm⁻¹ at 30 °C and 29.29 mS cm⁻¹ at 80 °C, making them promising candidates for fuel cell applications. Full article

N-phenyl-1H-Indole-5-carboxamide (Ind-CA) exhibits previously unknown room-temperature phosphorescence (RTP) when immobilized in poly (vinyl alcohol) film (PVA film). High-fluorescence anisotropy of Ind-CA in PVA suggests that the fluorophores are strongly immobilized in a polymer matrix, while a relatively low (ca. 0.1) quantum yield indicates a strong non-radiative singlet excited state deactivation. With an increased triplet-state population, Ind-CA can be used for various phosphorescence studies. The room-temperature phosphorescence (RTP) capability of Ind-CA indicates that there is an intricate balance between RTP and the structure of the indole-containing luminophore, as an isomeric N-1H-indole-5-ylbenzamide (Ind-BA) does not show any appreciable levels of RTP. Moreover, the phosphorescence lifetime of Ind-CA is about two orders of magnitude longer than many other 5-substituted indoles. These results further highlight the prospects for the potential rational designs of small molecules with desired triplet-state configuration and RTP characteristics. Full article

This review article focuses on providing an accumulated knowledge on state-of-the-art composite polymer coating technologies that are studied for corrosion protection. A specific focus has been given to epoxy resin-based composite systems, considering their wide use due to remarkable chemical resistance, excellent adhesion to substrate, thermal stability, and mechanical strength. The addition of various functional polymers to the epoxy matrix has spurred significant advancements in the prevention of corrosion. Light has been shed on the epoxy resin composite systems that are produced by blending with functional polymers like conductive polymers, hydrophobic polymers, etc., and nanofillers. In many cases, the formation of a passive layer at the metal/polymer interface was aided by the addition of such a functional polymer and nanofiller to the epoxy matrix. As a result, corrosive ions are prevented from penetrating by the physical barrier that composite coatings provide. Comparable blends of epoxy and polyamide, epoxy and polyester, and epoxy/poly(vinyl alcohol) and epoxy/polyurethane have superior adhesion, wear, barrier, and anticorrosion properties due to the fine dispersion of nanocarbon and inorganic nanoparticles. The several strategies used to prevent metals from corroding are covered in this review article. Full article

Most existing polymer plastics are nonreusable and also exhibit poor biocompatibility and a poor mechanical strength–tensile strain balance. Herein, using deep eutectic polymers, we prepare reusable hydrophilic supramolecular dry gel plastics with balanced stress–strain characteristics through the hydrogen bonding of poly(vinyl alcohol) (PVA) with betaine (Bta). As PVA exhibits crystalline stiffness and abundant hydrogen-bonding sites, it is employed as a network backbone in the proposed deep eutectic supramolecular polymers. In the prepared PVA/Bta dry gel plastics, PVA and Bta are dynamically and physically crosslinked through high-density hydrogen bonding, resulting in a yield strength of ~109 MPa and toughness of up to ~210.92 MJ m⁻³. In addition, these plastics can be recycled at least five times in an aqueous environment while maintaining a mechanical strength of 100 MPa. Furthermore, the proposed polymers exhibit high transparency (92%) in the visible spectrum. We expect these polymers to be used in synthesizing biodegradable dry gel plastics, as well as to lead to the development of recyclable deep eutectic PVA/Bta polymers with remarkable strength. Full article

This investigation of hydroxyl and polysiloxane absorption peaks in elastic polymer composites reveals significant spectral shifts within the fingerprint region of FTIR spectra. Using poly(vinyl butyral) (PVB) as the base polymer and poly(vinyl acetate) (PVAc) and poly(vinyl alcohol) (PVA) as reference materials, solvent effects on polymer–solvent interactions were systematically analyzed. Among the tested alcohol solvents, PEG 400 induced the most pronounced spectral changes, with the C=O stretching band shifting from 1740 to 1732 cm⁻¹ and the O–H band significantly broadening and downshifting to around 3300 cm⁻¹, reflecting strong hydrogen-bonding interactions. Wavelet-based noise reduction effectively enhanced the signal-to-noise ratio, reducing the baseline standard deviation by over 90%. This study introduces a novel noise-enhanced FTIR recognition model that integrates baseline noise metrics to improve detection sensitivity. The model successfully uncovers subtle structural variations in polymer–solvent systems that are typically masked by conventional FTIR techniques, advancing materials analysis and providing a robust framework for future FTIR-based diagnostics and material characterization. Full article

Current hydrogels used for cartilage tissue engineering often lack the mechanical strength and structural integrity required to mimic native human cartilage. This study addresses this limitation by developing reinforced hydrogels based on a ternary polymer blend of poly(vinyl) alcohol (PVA), gelatin (GL), and chitosan (CH), with gentamicin sulfate (GS) as an antimicrobial agent and a crosslinker. The hydrogels were produced using two crosslinking methods, the freeze/thaw and heated cycles, and reinforced with forcespun polycaprolactone (PCL) nanofiber to improve mechanical performance. Chemical characterization revealed that GS forms weak hydrogen bonds with the ternary polymers, leading to esterification with PVA, and covalent bonds are formed as the result of the free amino group (-NH₂) of chitosan that reacts with the carboxylic acid group (-COOH) of gelatin. SEM images help us to see how the hydrogels are reinforced with polycaprolactone (PCL) fibers produced via force spinning technology, while mechanical properties were evaluated via uniaxial tensile and compressive tests. Water retention measurements were performed to examine the crosslinking process’s influence on the hydrogel’s water retention, while the hydrogel surface roughness was obtained via confocal microscopy images. A constitutive model based on non-Gaussian strain energy density was introduced to predict experimental mechanical behavior data of the hydrogel, considering a non-monotonous softening function. Loading and unloading tests demonstrated that GS enhanced crosslinking without compromising water retention or biocompatibility because of the reaction between the free amino group of CH and the carboxylic group of gelatin. The PCL-reinforced PVA/GL/CH hydrogel shows strong potential for cartilage repair and tissue engineering applications. Full article

Nanostructured drug-delivery systems with enhanced therapeutic potential have gained attention in biomedical applications. Here, flufenamic acid (FFA)-loaded chitosan/poly(vinyl alcohol) (CHS/PVA; CSPA)-based electrospun nanofibers were fabricated and characterized for antibacterial, anticancer, and antioxidant activities. The FFA-loaded CSPA (FCSPA) nanofibers were characterized by scanning electron microscopy, Fourier-transform infrared spectroscopy, X-ray diffraction (XRD), and differential scanning calorimetry to evaluate their formation process, functional group interactions, and crystallinity. Notably, the average diameter of FCSPA nanofibers decreased with increasing CSPA contents (CSPA-1 to CSPA-3), indicating that FFA addition to CSPA-3 significantly decreased its diameter. Additionally, XRD confirmed the dispersion of FFA within the CSPA amorphous matrix, enhancing drug stability. FCSPA nanofibers exhibited a high swelling ratio (significantly higher than that of the CSPA samples). Biodegradation studies revealed that FCSPA exhibited accelerated weight loss after 72 h, indicating its improved degradation compared with those of other formulations. Furthermore, it exhibited a significantly high drug-encapsulation efficiency, ensuring sustained release. FCSPA nanofibers exhibited excellent antibacterial activity, inhibiting Staphylococcus aureus and Escherichia coli. Regarding anticancer activity, FCSPA decreased HCT-116 cell viability, highlighting its controlled drug-delivery potential. Moreover, FCSPA demonstrated superior antioxidation, scavenging DPPH free radicals. These findings highlight FCSPA nanofibers as multifunctional platforms with wound-healing, drug-delivery, and tissue-engineering potential. Full article