Search Results (1,444)

Background/Objectives: Although significant advances in duodenoscope reprocessing have been introduced since mid-2010s—including enhanced cleaning protocols, disposable distal endcaps, and the introduction of fully single-use duodenoscopes—residual contamination and infection risks remain unresolved. Moreover, repeated reprocessing may cause cumulative damage to the polymer surfaces, elevator mechanisms, and internal channels of the duodenoscopes, making them more susceptible to residual contamination. To minimize the duodenoscope polymer degradation caused by intensive use and reprocessing, new alternatives are urgently needed. In this context, calcium peroxide nanoparticles coated with sodium alginate (CaO₂–Alg NPs), synthesized by our group, were tested for the first time as a disinfectant capable of combating nosocomial pathogens while reducing device deterioration associated with repeated investigations and reprocessing. Methods: The disinfectant properties of the CaO₂–Alg NPs were evaluated under biomimetic conditions using reference bacterial strains commonly associated with nosocomial infections. In addition, the compatibility of the nanoparticles with the polymeric duodenoscope coatings was assessed after simulated intensive use. The external polymer coating was structurally and morphologically characterized by Fourier Transform Infrared Spectroscopy (FTIR), Differential Scanning Calorimetry (DSC), Atomic Force Microscopy (AFM), and Scanning Electron Microscopy (SEM). Results: The nanoparticles exhibited important antimicrobial activity against the reference bacterial strains Staphylococcus aureus, Escherichia coli, Enterococcus faecalis, and Klebsiella pneumoniae after only 20 min of incubation. Intensive exposure to the CaO₂–Alg NPs did not cause additional structural or morphological damage to the duodenoscope’s external polymers and did not alter their anti-adhesive properties. Conclusions: The CaO₂–Alg NPs appear to be a safe and effective disinfectant for the duodenoscope reprocessing, offering both antimicrobial efficacy and material compatibility. Full article

A versatile, sustainable feedstock pathway to bio-based polymeric materials was developed utilizing lignin biomass and the ring-opening copolymerization (ROCOP) of cyclic anhydrides and epoxides to synthesize functional, lignin-derived, fully bio-based polyester polyols. The initial goal was to make the ROCOP reaction more applicable to bio-derived starting materials and more attractive to commercialization by conducting the polymerization under less constrained and industrially relevant conditions in air and without the extensive purification of reagents, catalysts, or solvents, typically used in the literature. A refined ROCOP system was applied as a powerful tool in lignin valorization by successfully synthesizing the lignin-derived copolyester prepolymers from lignin models and depolymerized native lignin sourced from the reductive catalytic fractionation of Pinus radiata wood biomass. After mechanistic studies based on NMR characterization, an alternative ROCOP-style mechanism was proposed. This was found to be (1) contributing to the acceleration of the observed reaction rates with added [PPNCl] organo-catalyst and (2) ‘self-initiation/self-promoted’ ROCOP without any added external [PPNCl] catalyst, likely due to the presence of inherent [OH] groups/ species in the lignin-derived glycidyl ether monomer promoting reactivity. As a final goal, the potential of these lignin-derived polyesters as intermediate polyols was demonstrated by applying them in the synthesis of polyurethane (PU) film materials with a high biomass content of 75–79%. A dramatic range of thermomechanical properties was observed for the resulting materials, demonstrating how the ROCOP reaction can be used to tailor the properties of the functional polyester and PU material based on the nature of the epoxide and anhydride substrates used. These findings help endeavors towards predicting the relationship between chemical structure and material thermomechanical properties and performance, relevant for industrial applications. Overall, this study demonstrated the proof of concept that PU materials can be prepared from lignocellulosic biomass utilizing industrially feasible ROCOP of bio-derived cyclic anhydrides and epoxides. Full article

Although resin-based composite is the most popular direct restoration material in the U.S., composite restorations can fail shortly after placement. The leading cause of failure is recurrent marginal decay. The adhesive that bonds the composite to the tooth is intended to seal the margin, but the degradation of the adhesive seal to dentin leads to gaps that are infiltrated by cariogenic bacteria. The development of strategies to mitigate adhesive degradation is an area of intense interest. Recent studies focus on exploiting hydrogen–bond interactions to enhance polymer network stability. This paper presents the preparation and characterization of model adhesives that capitalize on carbamate-functionalized long-chain silane monomers to enhance polymer stability and mechanical properties in wet environments. The adhesive composition is HEMA/BisGMA, 3-component photoinitiator system, carbamate-functionalized long-chain silane monomers, e.g., commercial SHEtMA (Cb1) and newly synthesized SHEMA (Cb2). Polymerization behavior, water sorption, leachates, and dynamic mechanical properties were investigated. The properties of Cb1 and Cb2 were compared to previously studied middle- (SC4) and short-chain (SC5) silane monomers. Cb1- and Cb2-formulations exhibit greater resilience under wet conditions as compared to middle-chain silane monomers. Dental adhesives containing the carbamate-functionalized long-chain silane monomers exhibit reduced flexibility in water-submersed conditions and enhanced stability as a result of increased hydrogen–bond interactions. The results emphasize the critical role of hydrogen bonding in maintaining structural integrity of dental adhesive formulations under conditions that simulate the wet, oral environment. Full article

To evaluate the creep and fatigue fracture lives of structural acrylic spliced components fabricated via bulk polymerization, and to elucidate the associated fracture mechanisms, this study conducted creep and fatigue tests on spliced coupons annealed at 85 °C and 65 °C, as well as base material coupons. The experimental life data were fitted using log-log linear regression models. Based on statistical analysis, a simple yet robust statistical framework was established for life prediction, featuring three design curves: 97.7% survival curves, improved 95% confidence interval lower bounds, and one-sided tolerance curves. Fractographic examination using scanning electron microscopy (SEM) was performed to characterize macroscopic failure modes. The results indicate distinct threshold behavior between stress levels and both creep and fatigue life. The creep threshold stresses are 25 MPa for the base material, 29 MPa for the spliced coupons annealed at 85 °C, and 17 MPa for the spliced coupons annealed at 65 °C. Corresponding fatigue threshold stress amplitudes are 21 MPa, 22 MPa, and 31 MPa, respectively. Failure in the base material is primarily initiated by randomly distributed internal defects, whereas failure in the spliced coupons is mainly caused by defects within the seam or interfacial tearing. Full article

Cannabidiol (CBD) and its derivatives show interesting therapeutic potential, including antioxidant, anti-inflammatory, and anticancer properties; however, their clinical translation remains a complex task due to physicochemical restrictions such as low water solubility, high lipophilicity, and instability under light, oxygen, and high temperatures. Polymeric encapsulation has emerged as a promising strategy to overcome these challenges, offering protection against environmental degradation, improved bioavailability, and controlled release. Natural and synthetic polymers, both biocompatible and biodegradable, provide versatile matrices for CBD delivery, enabling nanoparticle formation, targeted transport, and enhanced pharmacokinetics. This review highlights the structural characteristics of CBD, its interaction mechanisms with polymeric matrices such as hydrogels, electrospun nanofibers, biodegradable microparticles, thin films, and lipid-polymer hybrid systems, and the principal encapsulation techniques, such as emulsion solvent evaporation, electrospinning, and supercritical fluid technologies, that facilitate stability and scalability. Furthermore, material characterization approaches, including microscopy, thermal, and degradation analyses, are discussed as tools for optimizing encapsulation systems. While notable advances have been made, key challenges remain in achieving reproducible large-scale production, ensuring regulatory compliance, and designing smart polymeric carriers personalized for specific therapeutic contexts. By addressing these gaps, polymer-based encapsulation may unlock new opportunities for CBD in pharmaceutical, nutraceutical, and therapeutic applications, providing a guide for future innovation and translation into effective patient-centered products. Full article

This work aims to apply polymeric PBAT/PLA fibers electrospun with TiO₂ in the photodegradation of the dye Red BF-4B in an aqueous solution and the dye’s subsequent reuse. Initially, the influence of the solution pH was evaluated, and the results showed more significant dye degradation at pH values below the pHpcz (7.42). Kinetic studies show that at 15 mg·L⁻¹, the highest percentage of degradation occurs at 600 min of reaction time; however, degradation equal to (or greater than) 65% was observed at all evaluated concentrations, with the kinetic data being well fitted by the pseudo-first-order model. Additional studies demonstrated the reuse of polymeric films for dye removal, with removal efficiencies ranging from 86.60% to 93.07% over six consecutive reuse cycles. Each cycle consisted of a 600 min removal process, simulating repeated practical applications. After the photocatalytic process, the polymeric fibers remained cylindrical, with several fractures. Diameter decreases of 31.61% and 7.95% were observed after the first and sixth cycles, respectively, with possible exposure of TiO₂. The vibrational spectra indicate changes in the bands at 1755 and 1714 cm⁻¹, attributed to C=O (PLA) and C-O (PBAT) stretches, respectively, suggesting a possible conformational change in the polymers. The thermal profiles showed only slight changes after the cycles. X-ray diffractograms indicate that degradation of the polymeric matrix leads to greater exposure of the embedded TiO₂ particles. The combined results from different characterization techniques provide evidence of the degradation of the polymeric material. Full article

Polymeric optical waveguides represent an essential component in photonic technology thanks to their ability to guide light through controlled structures, enabling applications in telecommunications, sensors, and integrated devices. With the development of new materials and increasingly versatile manufacturing methods, these structures are being integrated into various systems at a rapid pace, while their dimensions are constantly being reduced. This article explores the main fabrication methods for polymeric optical waveguides, such as traditional and maskless photolithography, laser ablation, hot embossing, nanoimprint lithography, the Mosquito method, inkjet printing, aerosol jet printing, and electrohydrodynamic (EHD) printing. The operating principle of each method, the equipment and materials used, and their advantages, limitations, and practical applications are evaluated, in addition to the propagation losses and characterization of the waveguides obtained with each method. Full article

To address critical limitations of ultra-low viscosity supercritical CO₂ fracturing fluids, including excessive fluid loss and inadequate proppant transport capacity, a series of thickeners designed to significantly enhance CO₂ viscosity were synthesized. Initially, FT-IR and ¹H NMR characterization confirmed successful chemical reactions and incorporation of both solvation-enhancing and -thickening functional groups. Subsequently, dissolution and thickening performance were evaluated using a custom-designed high-pressure vessel featuring visual observation capability, in-line viscosity monitoring, and high-temperature operation. All thickener systems exhibited excellent solubility, with 5 wt% loading elevating CO₂ viscosity to 3.68 mPa·s. Ultimately, molecular simulations performed in Materials Studio elucidated the mechanistic basis, electrostatic potential (ESP) mapping, cohesive energy density analysis, intermolecular interaction energy, and radial distribution function comparisons. These computational approaches revealed dissolution and thickening mechanisms of polymeric thickeners in CO₂. Full article

In this work, pCh-MWCNTs@Ag-TiO₂/S and pCh-MWCNTs@Ag-TiO₂ nanocomposites were synthesized through a combined phosphorylation and cross-linked polymerization method. The materials were thoroughly characterized using several analytical techniques, including SEM/EDS, FTIR, TGA, and BET analysis. SEM images revealed that the pCh-MWCNTs@Ag-TiO₂/S nanocomposite displayed a smooth, flake-like morphology with spherical, dark greenish particles. EDS analysis confirmed the presence of Si, S, P, and Ag as prominent elements, with Ti, C, and O showing the most intense peaks. The TGA curves indicated significant weight loss between 250–610 °C for pCh-MWCNTs@Ag-TiO₂ and 210–630 °C for pCh-MWCNTs@Ag-TiO₂/S, corresponding to the decomposition of organic components. FTIR spectra validated the existence of functional groups such as hydroxyl (-OH), carboxyl (-COOH), and carbonyl (-C=O) on the surface of the nanocomposites. Following characterization, the materials were evaluated for their capacity to adsorb Hg²⁺ at parts-per-billion (ppb) concentrations in contaminated water. Batch adsorption experiments identified optimal conditions for mercury removal. For pCh-MWCNTs@Ag-TiO₂, the best performance was observed at pH 4, with an adsorbent dose of 4.0 mg, initial mercury concentration of 16 ppb, and a contact time of 90 min. For pCh-MWCNTs@Ag-TiO₂/S, optimal conditions were at pH 6, a dosage of 3.5 mg, the same initial concentration, and a contact time of 100 min. Each parameter was optimized to determine the most effective conditions for Hg²⁺ removal. The nanocomposites showed high efficiency, achieving more than 95% mercury removal under these conditions. Kinetic studies indicated that the adsorption process followed a pseudo-second-order model, while the equilibrium data aligned best with the Langmuir isotherm, suggesting monolayer adsorption behavior. Overall, this research highlights the effectiveness of sulfur-modified chitosan-based nanocomposites as eco-friendly and efficient adsorbents for the removal of mercury from aqueous systems, offering a promising solution for water purification and environmental protection. Full article

Surface roughness influences biofilm adhesion on denture base materials, impacting oral health. Despite advances in polymeric denture materials, the effects of common cleaning protocols on their surface texture remain inadequately characterized. This study investigated the influence of toothbrush abrasion on the surface texture of dimethyl methacrylate-based (DMA, printed: V-Print dentbase), polymethyl methacrylate (PMMA, milled: VITA Vionic Base, pressed: IvoBase Hybrid), polyamide (PA, pressed: Bre.flex), and polyether ether ketone (PEEK, milled: Juvora Disc). The specimens were fabricated as polished discs. The Vickers and Martens hardness, indentation modulus, elastic and plastic part of indentation work, and indentation creep were determined. Toothbrushing simulation and surface texture analysis were conducted in three steps: 1800, 1800, and 3600 cycles using water, dish detergent, or toothpaste slurry. The surface texture parameters Sa, Sal, Sdr, Sku, and Ssk were determined using confocal laser scanning microscopy and suitable filtering (S-F and S-L surface). Sa, Sal, and Sdr showed significant changes depending on the choice of medium and the material used. The duration had a small effect (three-way ANOVA; all p < 0.001). DMA showed minor surface changes. Milled and pressed PMMA exhibited similar surface deformities due to wide valleys that were not considered critical for biofilm adhesion. PA showed the lowest and PEEK the highest Vickers and Martens hardness. However, both PA and PEEK exhibited surface changes that could promote biofilm development. These findings suggest that denture cleaning recommendations should remain material-specific. Regular surface inspections and repolishing are necessary to reduce the risk of biofilm formation on PA or PEEK-containing dentures. Full article

In this study, a novel LFP–catalytic microfiltration membrane (LFP@PVDF) was fabricated by loading a lithium-ion battery material LiFePO₄ (LFP) onto polymeric micro-porous polyvinylidene fluoride (PVDF) using a filter press coating method. The successful loading of LFP material onto the LFP@PVDF catalytic membrane was confirmed by the characterization of the material using FTIR, SEM, EDX, and XRD analysis. To evaluate the catalytic performance of the LFP@PVDF membrane, the reactive black 5 (RB5) dye-containing solution was used with or without the peroxymonosulfate (PMS) activator in a dead-end filtration under room conditions. The influence of parameters such as LFP loading, initial RB5 dye concentration, persulfate dosage, and solution pH on the performance of the persulfate oxidation process was comprehensively examined. It was found that the LFP@PVDF membrane/persulfate activation system can effectively remove RB5 dye with an efficiency of 97.3%. The RB5 dye removal by LFP@PVDF membranes with varying experimental conditions was found to fit the pseudo-second-order kinetic model. Quenching experiments showed that the reactive species ${\mathrm{HO}}^{•}$, ${{\mathrm{SO}}_4}^{•-}$ and ¹O₂ were responsible for the dye removal. The LFP@PVDF membrane/persulfate activation system appeared to be a promising approach for the removal of organic contaminants. Full article

A novel quinoline-containing benzoxazine resin, 8HQ-fa, has been successfully synthesized at room temperature using sustainable raw materials, such as 8-hydroxyquinoline and furfurylamine as the phenol and amine source, respectively. The chemical structure of the hereinafter referred to as quinolinoxazine is fully characterized by Fourier transform infrared spectroscopy (FT-IR), ¹H and ¹³C nuclear magnetic resonance spectroscopy (NMR), as well as by 2D ¹H–¹H nuclear Overhauser effect spectroscopy (NOESY) and ¹H–¹³C heteronuclear multiple quantum correlation (HMQC) NMR. Thermal properties and polymerization behavior of the monomer are studied by differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The resulting polymer is also characterized in terms of its thermal and fire-related properties by DSC, TGA, and microscale combustion calorimetry (MCC). The resulting thermoset, poly(8HQ-fa), presents good thermal stability as evidenced by its T_g (201 °C), T_d5 and T_d10 (307 and 351 °C, respectively), and char yield (42%), and low flammability as determined by the LOI, heat release capacity, and total heat released values (34.3, 143 J/gK, and 10.8 kJ/g, respectively), making it a self-extinguishing thermoset. The combination of properties and advantages in the synthesis of 8HQ-fa, accompanied by a low polymerization temperature, suggests its great potential in the field of high-performance polymers. Full article

Adhering to the principles of green analytical chemistry (GAC) is crucial for advancing sample pretreatment. In this work, we developed a green in-tube solid-phase microextraction (IT-SPME) material utilizing non-toxic cyclodextrin and zwitterionic polymers as co-functioning monomers. The hybrid monolithic material was synthesized within 38 min via an efficient epoxy ring-opening reaction and free radical polymerization. Comprehensive characterization confirmed a rigid framework with strong anti-swelling properties, good permeability, and high enrichment efficiency on the polymers. When coupled with HPLC-UV, the optimized IT-SPME method enabled highly sensitive detection of polypeptides (vancomycin and teicoplanin) in aqueous matrices, achieving detection limits as low as 15.0–20.0 μg L⁻¹, a wide linear range (60–800 μg L⁻¹, R² > 0.99), and good precision (RSDs = 5.9–8.2%). The prepared material demonstrated remarkable performance in real complex water samples, achieving recovery rates of up to 95.4%. Density functional theory (DFT) calculations indicated that the adsorption mechanism primarily involves hydrogen bonding and electrostatic interactions. This study presents an effective approach for the development of green chemical synthesis of extraction materials and offers a sustainable platform for monitoring trace contaminants in environmental waters. Full article

Functional hydrogels are a growing class of soft materials. Functional hydrogels are characterized by their three-dimensional (3D) polymeric network and high water-retention capacity. Functional hydrogels are deliberately engineered with specific chemical groups, stimuli-responsive motifs, or crosslinking strategies that impart targeted biomedical or environmental roles (e.g., drug delivery, pollutant removal). Their capacity to imitate the extracellular matrix, and their biocompatibility and customizable physicochemical properties make them highly suitable for biomedical and environmental applications. In contrast, non-functional hydrogels are defined as passive polymer networks that primarily serve as water-swollen matrices without such application-oriented modifications. Recent progress includes stimuli-responsive hydrogel designs. Stimuli such as pH, temperature, enzymes, light, etc., enable controlled drug delivery and targeted therapy. Moreover, hydrogels have shown great potential in tissue engineering and regenerative medicine. The flexibility and biofunctionality of hydrogels improve cell adhesion and tissue integration. Functional hydrogels are being explored for water purification by heavy metal ion removal and pollutant detection. The surface functionalities of hydrogels have shown selective binding and adsorption, along with porous structures that make them effective for environmental remediation. However, hydrogels have long been postulated as potential candidates to be used in clinical advancements. The first reported clinical trial was in the 1980s; however, their exploration in the last two decades has still struggled to achieve positive results. In this review, we discuss the rational hydrogel designs, synthesis techniques, application-specific performance, and the hydrogel-based materials being used in ongoing clinical trials (FDA–approved) and their mechanism of action. We also elaborate on the key challenges remaining, such as biocompatibility, mechanical stability, scalability, and future directions, to unlocking their multifunctionality and responsiveness. Full article

This work describes the synthesis and characterization of novel organometallic polymeric frameworks derived from lactone-based poly(benzofuran-co-arylacetic acid) (PBAAA) ligands complexed with 3d transition metal salts (Co²⁺, Cu²⁺, Zn²⁺). Two distinct synthetic approaches were investigated: conventional solution-based methods and mechanochemical ball milling. A comprehensive spectroscopic evaluation was performed utilizing FTIR, XRD, UV-Vis, and XPS techniques to detail the structural characteristics of the synthesized materials. The thermal assessments were conducted using TGA and thermal conductivity, demonstrating that the chosen synthesis method has a significant impact on the crystallinity, coordination environment, and thermal transport characteristics of the resultant complexes. Remarkably, using the mechanosynthesis, the resulting organometallic polymer materials exhibited enhanced chain ordering and improved thermal conductivity, with a value of 0.32 W/mK, almost double that of the starting polymer. A correlation was identified among thermal conductivity, metal ionic radius, coordination number, and the synthesis method utilized. XPS analysis revealed the presence of multiple oxidation states and varied electronic environments, particularly in copper complexes. These had a direct effect on how they behaved when heated. These results show that mechanochemical synthesis is a useful and long-lasting method to make complex organometallic polymers with thermal properties that can be changed. Full article