Search Results (1,567)

The rheological behavior and low-temperature curing kinetics of poly(ethylene glycol fumarate)–acrylic acid systems initiated by benzoyl peroxide/N,N-dimethylaniline have been investigated for the first time with a focus on the development of thermosetting binders with controllable properties. It has been established that both composition and temperature have a significant effect on rheological behavior and kinetic parameters. Rheological studies revealed non-Newtonian flow behavior and thixotropic properties, while oscillatory tests demonstrated structural transformations during curing. Increasing the temperature was found to accelerate gelation, whereas a higher polyester content retarded the process, which is crucial for controlling the pot life of the reactive mixture. DSC analysis indicated that isothermal curing at 30–40 °C can be satisfactorily described by the Kamal autocatalytic model, whereas at 20 °C, at later stages, and at higher polyester contents, diffusion control becomes significant. The thermal behavior of cured systems was investigated using thermogravimetry. Calculations using the isoconversional Kissinger–Akahira–Sunose and Friedman methods confirmed an increase in the apparent activation energy for thermal decomposition, suggesting a stabilizing effect of poly(ethylene glycol fumarate) in the polymer structure. The studied systems are characterized by controllable kinetics, tunable viscosity, and high thermal stability, making them promising thermosetting binders for applications in composites, construction, paints and coatings, and adhesives. Full article

The precipitation of cellulose and polyacrylonitrile and its copolymer (PAN) solutions is a well-known process that has been extensively described in numerous studies. It is suggested that “soft” precipitants (aqueous solutions of solvent, alcohols) be used in place of “rigid” ones (water) to control the rate at which solutions precipitate. Diffusion processes can also be controlled by lowering the temperature of the interacting system’s constituent parts. The appearance and structure of the resulting fibers (films) are directly correlated with the rate of coagulation. Adding a composite additive to the solution is an unusual method of altering the rate of polymer phase release. The introduced additive should dissolve in a common solvent, which will ensure the competition of precipitation between the polymer phases. It is shown that using optical methods it is possible to trace the evolution of the polymer phase precipitation and the formed morphology. For 12% solutions of cellulose, PAN and mixed systems in N-methylmorpholine-N-oxide (NMMO) the kinetics of the movement of isoconcentration planes was traced and the growth rates of the precipitated polymer zone were estimated. The introduction of PAN additives into cellulose enables the influence of diffusion processes and minimizes the formation of finger-like defects (vacuoles). When the PAN content in the system is 30% or more, the formation of defects in the precipitated solution is significantly suppressed, which is crucial for achieving a uniform morphology. Full article

Background/Objectives: Semi-solid extrusion (SSE) three-dimensional (3D) printing offers a versatile approach for fabricating personalized oral dosage forms. This study aimed to develop and optimize losartan potassium tablets produced via SSE 3D printing, focusing on the effects of polymer composition, tablet geometry, drug loading, and superdisintegrant concentration on printability and performance characteristics. Methods: Formulations containing hydroxypropyl methylcellulose (HPMC) 4500 at various concentrations were evaluated for suitability in an ethanol–water (9:1 v/v) solvent system. The optimized formulation (5% w/w HPMC 4500) was used to print tablets with varying shapes, drug loadings (5–15% w/w; approximately 50–150 mg losartan potassium per tablet), and croscarmellose sodium concentrations (0–3% w/w). Printed tablets were characterized for dimensional accuracy, mass uniformity, disintegration time, and drug release behavior. Drug release kinetics were modeled to elucidate the release mechanism. Results: All SSE-printed tablets exhibited excellent dimensional precision (SD < 0.8 mm) and mass uniformity (SD < 0.12 g). Increasing drug loading enhanced the initial release rate, reaching up to 63% in 45 min for 15% loading. The addition of 1% croscarmellose sodium reduced disintegration time to approximately 25 min. Drug release profiles were best described by the Korsmeyer–Peppas model (R² > 0.96), indicating diffusion-controlled release. Conclusions: SSE 3D printing demonstrated robustness and flexibility in producing losartan potassium tablets with consistent quality, tunable release properties, and strong potential for personalized pharmaceutical manufacturing. Full article

Highly permeable and selective membranes are crucial for energy-efficient gas separation. Two-dimensional (2D) graphitic carbon nitride (g-C₃N₄) has attracted significant attention due to its unique structural characteristics, including ultra-thin thickness, inherent surface porosity, and abundant amine groups. However, the interfacial defects caused by poor compatibility between g-C₃N₄ and polymers deteriorate the separation performance of membrane materials. In this study, amino-functionalized g-C₃N₄ nanosheets (CN@PEI) was prepared by a post-synthesis method, then blended with the polymer Pebax to fabricate Pebax/CN@PEI mixed matrix membranes (MMMs). Compared to g-C₃N₄, MMMs with CN@PEI loading of 20 wt% as nanofiller exhibited a CO₂ permeance of 241 Barrer as well as the CO₂/CH₄ and CO₂/N₂ selectivity of 39.7 and 61.2, respectively, at the feed gas pressure of 2 bar, which approaches the 2008 Robeson upper bound and exceeded the 1991 Robeson upper bound. The Pebax/CN@PEI (20) membrane showed robust stability performance over 70 h continuous gas permeability testing, and no significant decline was observed. SEM characterization revealed a uniform dispersion of CN@PEI throughout the Pebax matrix, demonstrating excellent interfacial compatibility between the components. The increased free volume fraction, enhanced solubility, and higher diffusion coefficient demonstrated that the incorporation of CN@PEI nanosheets introduced more CO₂-philic amino groups and disrupted the chain packing of the Pebax matrix, thereby creating additional diffusion channels and facilitating CO₂ transport. Full article

Y₂O₃ nanoparticles were used in a polyethersulfone (PES) as additives to increase the permeation properties of the polymeric membranes. Membranes were manufactured by diffusion-induced phase inversion in N-methyl-pyrrolidone (NMP) using a different concentration of nanoparticles. Y₂O₃ is used in polymeric membranes to enhance their functional properties, especially in wastewater treatment processes. Incorporating Y₂O₃ nanoparticles into the polymer matrix improves the membrane’s hydrophilicity, permeability, and mechanical strength. Additionally, Y₂O₃ provides better properties and reduces fouling. Recent studies highlight its potential as a modifying agent for advanced composite membranes. This paper investigated challenges in the synthesis of Y₂O₃-enhanced membranes and links synthesis with performance. It was observed that the composite membranes have better permeation properties by adding a small amount of Y₂O₃. For membranes at 21 wt.% PES permeability increase from 107 to 112 L/m²·h/bar. Fouling performance increases by adding nanoparticles, relative flux decreases by 30% for membranes without nanoparticles and by 10% for membranes with nanoparticles, both at a concentration of 25% PES. Rejection increases for membranes at 21%Pes from 21% for membranes without nanoparticles to 39% for membranes with nanoparticles. The influence of Y₂O₃ nanoparticles on the membranes’ performance was determined by filtration experiments to establish the permeability, fouling, retention, and the water flux; by contact angle to establish the surface hydrophilicity; and by SEM to investigate the membranes’ structures. Full article

This study explores the drying kinetics and film formation behavior of polyvinyl alcohol (PVA)-based and PVA–bentonite composite coatings with initial thicknesses of approximately 2500 µm and 2000 µm. Four coating formulations were investigated, varying in PVA concentration and presence of bentonite as an inorganic filler. The drying process was monitored through changes in solid concentration, residual solvent content, and film thickness over time. Results revealed that coatings with higher PVA content exhibit slower drying rates, due to the transition from evaporation-controlled to diffusion-limited mechanisms, attributed to polymer densification and reduced solvent diffusivity. In contrast, coatings incorporating bentonite dried more rapidly despite their similar or higher total solids content, indicating a beneficial role of bentonite in facilitating moisture transport. Thinner coatings demonstrated faster drying but retained the characteristic mechanistic transitions observed in thicker films. A simple realistic model to simulate the drying rate was also proposed. Overall, the study highlights the significant influence of formulation variables on drying behavior and final film properties, offering valuable guidance for the design and optimization of waterborne coatings in industrial applications. Full article

Polyethylene furanoate (PEF) and Tritan^TM copolyester are sustainable polyester polymers. PEF is made from biobased resources, whereas Tritan is mainly used for reusable food contact articles. Both polyesters are alternatives for polyethylene terephthalate (PET), which is currently the most used polyester in food packaging. Like all packaging polymers, sustainable alternatives to fossil-based PET must also comply with food law requirements. Prediction of the migration can be used as an alternative to complex and time-consuming experimental migration measurements. Since there are no such predictive models for either PEF or Tritan, the modelling parameters for PEF and Tritan were determined in this study from experimentally determined diffusion coefficients and activation energies. The diffusivity of PEF and Tritan was compared with PET and polyethylene naphthalate (PEN). Of the four polyester polymers, PEF shows the lowest diffusion, followed by PEN, PET, and Tritan. Overall, the results show that the investigated polyesters are low-diffusivity polymers. Full article

Thick active layers are crucial for scalable production of organic photodetectors (OPDs). However, most OPDs with active layers thicker than 200 nm typically exhibit decreased photocurrents and responsivities due to exciton diffusion and prolonged charge transport pathways. To address these limitations, we designed and synthesized PFBDT-8ttTPD, a fluorinated polymer donor. The strategic incorporation of fluorine effectively enhanced the charge carrier mobility, enabling more efficient charge transport, even in thicker films. OPDs combining PFBDT−8ttTPD with IT−4F or Y6 non-fullerene acceptors showed a substantially lower dark current density (J_d) for active layer thicknesses of 250−450 nm. Notably, J_d in the IT-4F-based devices declined from 8.74 × 10⁻⁹ to 4.08 × 10⁻¹⁰ A cm⁻² under a reverse bias of −2 V, resulting in a maximum specific detectivity of 3.78 × 10¹³ Jones. Meanwhile, Y6 integration provided near-infrared sensitivity, with the devices achieving responsivity above 0.48 A W⁻¹ at 850 nm and detectivity over 10¹³ Jones up to 900 nm, supporting broadband imaging. Importantly, high-quality thick films (≥400 nm) free of pinholes or defects were fabricated, enabling scalable production without performance loss. This advancement ensures robust photodetection in thick uniform layers and marks a significant step toward the development of industrially viable OPDs. Full article

Developing highly permeable and selective membranes for energy-efficient CO₂/CH₄ separation remains challenging. Mixed-matrix membranes (MMMs) integrating polymer matrices with metal–organic frameworks (MOFs) offer significant potential. However, rational filler–matrix matching presents substantial difficulties, constraining separation performance. In this work, defects were engineered within fluorinated MOF ZU-61 through the partial replacement of 4,4′-bipyridine linkers with pyridine modulators, producing high-porosity HP-ZU-61 nanoparticles exhibiting a 267% BET surface area enhancement (992.9 m² g⁻¹) over low-porosity ZU-61 (LP-ZU-61) (372.2 m² g⁻¹). The HP-ZU-61/6FDA-DAM MMMs (30 wt.%) demonstrated homogeneous filler dispersion and pre-served crystallinity, achieving a CO₂ permeability of 1626 barrer and CO₂/CH₄ selectivity (33), surpassing the 2008 Robeson upper bound. Solution-diffusion modeling indicated ligand deficiencies generated accelerated diffusion pathways, while defect-induced unsaturated metal sites functioned as strong CO₂ adsorption centers that maintained solubility selectivity. This study establishes defect engineering in fluorinated MOF-based MMMs as a practical strategy to concurrently overcome the permeability–selectivity trade-off for efficient CO₂ capture. Full article

Hybrid polysaccharide-based aerogels offer significant potential as advanced drug delivery platforms due to their tunable structure, high porosity, and biocompatibility. In this study, aerogel microparticles were synthesized using alginate, pectin, carrageenan, and their hybrid formulations via an emulsion–gelation technique followed by supercritical fluid CO₂ extraction. The resulting aerogels exhibit mesoporous structures with specific surface areas ranging from 324 to 521 m²/g and pore volumes between 1.99 and 3.75 cm³/g. Comprehensive characterization (SEM, gas sorption, XRD, TGA, DSC, and FTIR) confirmed that hybridization improved morphological uniformity and thermal stability compared to single polymer aerogels. Ibuprofen was used as a model drug to evaluate loading efficiency and release kinetics. Among all formulations, the alginate/carrageenan (2:1) hybrid showed the highest drug loading efficiency (93.5%) and a rapid release profile (>90% within 15 min), closely matching the performance of commercial ibuprofen tablets. Drug release followed Fickian diffusion, as confirmed by the Korsmeyer–Peppas model (R² > 0.99). These results highlight the potential of hybrid polysaccharide aerogels as vehicles for drug delivery and other fast-acting therapeutic applications. Full article

Traditional chemical-based sanitizers pose risks to health and the environment, highlighting the need for safer natural alternatives. We developed biocompatible hydrogels from carbohydrate-based biopolymers, chitosan (1.5% and 2.5%), and carboxymethylcellulose (CMC, 3% and 5%), each incorporating one of four antimicrobials: microcin J25, nisin Z, pediocin PA-1, or reuterin. Hydrogels were prepared by dissolving the polymers in aqueous solution and incorporating antimicrobials before gelation. The formulations were characterized using viscosity measurements, antimicrobial assays, and stability testing over 28 days of storage at room temperature (23–25 °C). Chitosan hydrogels with microcin J25 maintained strong activity against Salmonella enterica ATCC 6962, while nisin Z retained activity in gel and solution forms, though with some decline during storage. Pediocin PA-1 remained active in 1.5% and 2.5% chitosan hydrogels against Listeria monocytogenes ATCC 19115, but activity was lost in 3% and 5% CMC hydrogels. Reuterin preserved activity in CMC-based hydrogels throughout storage. In solution, microcin J25 and nisin Z consistently achieved ~7-log reductions, whereas pediocin PA-1 and reuterin reached up to ~5-log reductions. In gels, efficacy decreased at lower concentrations and shorter contact times, likely due to diffusion barriers. Overall, the hydrogels remained stable during storage, and CMC- and chitosan-based matrices with selected antimicrobials show promise as alternatives to chemical sanitizers. Their application should be tailored to specific needs, with formulations requiring longer contact times best suited for surfaces that allow prolonged exposure. Full article

MOF-808 was synthesized using different (perfluoro)carboxylic acid modulators, including acetic acid (AA), butyric acid (BA), trifluoroacetic acid (TFAA) and heptafluorobutyric acid (HFBA). These samples were incorporated into co-polyimide 6FDA-DAM:DABA (6FDD), and the performance of the resulting MMMs was assessed for C₂ and C₃ olefin/paraffin separation. Enhanced permeability was observed for both C₂H₄/C₂H₆ and C₃H₆/C₃H₈ mixtures thanks to the introduced porosity upon filler incorporation in all cases. Due to the large pore size of MOF-808, diffusion-selective permeation through the polymer phase of the MMMs determined the eventual selectivity for C2 gases, leading to separation factors similar to that of the unfilled 6FDD membrane. For C₃H₆/C₃H₈ separation, the incorporation of fluorinated MOFs significantly improved separation performance, unlike their non-fluorinated counterparts. The unfilled 6FDD membrane exhibited a C₃H₆/C₃H₈ separation factor of 7.4 with a C₃H₆ permeability of 22 Barrer, while the incorporation of MOF-808-TFAA and MOF-808-HFBA led to C₃H₆/C₃H₈ separation factors of 13.1 and 13.5 with corresponding improved C₃H₆ permeabilities of 42 Barrer and 33 Barrer, respectively. Considering that these MMMs showed C₃H₆ permeabilities similar to those of MMMs containing their non-fluorinated MOF counterparts that exhibited no enhancement in membrane selectivity, the improved C₃H₆/C₃H₈ separation factor was attributed to the preferential adsorption of C₃H₈ over C3H6 on the fluorinated MOFs, acting as a trap for C₃H₈ and reducing its diffusivity. These results highlight the significance of matching the permeation characteristics of the selected polymer-filler pair on MMM performance for different gas pairs. Full article

We report a systematic investigation on the physicochemical properties of polymer systems consisting of polyvinyl alcohol (PVA) and hyaluronic acid (HA) mixed in various volume ratios (1/4, 2/3, 1/1, 3/2, and 4/1). At PVA/HA ratios above 1/1, in the presence of glutaraldehyde and divinyl sulfone as crosslinking agents, hydrogels are formed. Their swelling behavior is dependent on the polymer ratio, with the highest water uptake determined for PVA/HA 4/1. The in situ generation of reactive oxygen species (HO^• radicals) under UV-A irradiation, in the presence of riboflavin as a photoinitiator, is evidenced by electron paramagnetic resonance (EPR) spectroscopy. The diffusion of small paramagnetic molecules across the interface of two PVA/HA 4/1 gel pieces placed in direct contact reveals the occurrence of molecular exchange, which could indicate some degree of self-repair of the hydrogel network. When the paramagnetic moiety is attached to the HA polymer by spin labeling, the absence of diffusion demonstrates the stability of the crosslinked HA chains within the PVA/HA network. The structural modifications induced by crosslinking, by the presence of riboflavin, and by exposure to UV-A light, and the resulting alterations in the mechanical behavior of the hydrogels are monitored by infrared spectroscopy and rheology. Only a slight decrease in the viscoelastic moduli values is noted, indicating that the formation of HO^• radicals has minimal impact on the macroscopic properties of the hydrogels. Full article

Objective: This study aimed to evaluate the effect of incorporating bioactive particles (montmorillonite loaded with chlorhexidine, MMT/CHX) and different concentrations of silica nanoparticles (0%, 3%, 5%, 7%, 10%, and 15 wt%) into a universal dental adhesive on its degree of conversion, bond strength, water sorption, solubility, and antimicrobial activity. Materials and Methods: A universal adhesive was modified with 1 wt% MMT/CHX and varying amounts of silica nanoparticles. Degree of conversion was analyzed by Fourier transform infrared spectroscopy (FTIR), and microtensile bond strength was evaluated at 24 h, 6 months, and 12 months after water storage. Water sorption and solubility were measured according to ISO 4049, and antibacterial activity was tested against Streptococcus mutans using the agar diffusion method. Results: All experimental adhesives containing ≥7% silica showed significantly reduced water sorption and solubility. The presence of MMT/CHX imparted consistent antimicrobial activity across all experimental groups. Degree of conversion remained stable across all groups and storage periods. Notably, after 12 months, only the experimental groups maintained or improved bond strength, while the control group showed a significant reduction. Failure mode analysis indicated increased mechanical integrity with higher filler content. Conclusions: Incorporating 1 wt% MMT/CHX and ≥7 wt% silica into a universal adhesive improved long-term bond strength, reduced degradation, and introduced antibacterial properties without compromising polymer conversion. These findings support the potential of developing durable, bioactive adhesive systems for restorative dentistry. Clinical Significance: The incorporation of bioactive and reinforcing nanoparticles into universal adhesives enhances bond durability and introduces antibacterial properties without compromising polymerization. This innovation may lead to longer-lasting restorations and reduced risk of secondary caries in clinical practice. Full article

Tooth whitening is increasingly sought in both clinical and home settings, raising concerns about the efficacy and safety of various whitening agents and their delivery systems. This narrative review compares the whitening performance and biocompatibility of active ingredients, including hydrogen peroxide, carbamide peroxide, activated charcoal, sodium bicarbonate, fluoride compounds, and blue covarine, with particular emphasis on the role of polymer-based carriers in formulation strategies. Hydrogen peroxide and carbamide peroxide remain the most effective agents for intrinsic whitening, but are associated with risks of enamel surface alterations, microhardness reduction, and potential cytotoxicity, particularly at higher concentrations. Sodium bicarbonate provides moderate whitening effects through extrinsic stain removal, while fluoride compounds play a supportive role by reducing demineralization and tooth sensitivity, thereby preserving enamel integrity. These properties make them valuable adjuncts or alternatives for patients with high sensitivity risks. Blue covarine offers immediate optical effects without inducing intrinsic color changes, whereas activated charcoal poses risks of enamel abrasion and surface roughness with limited long-term efficacy. Polymer-based carriers such as Carbopol gels, polyvinylpyrrolidone, and hydroxypropyl methylcellulose are incorporated into whitening formulations to improve viscosity, adhesion, and modulate the release of active ingredients. These polymers might help minimize diffusion of bleaching agents into deeper dental tissues, potentially reducing cytotoxic effects, and may improve handling characteristics. However, dedicated studies evaluating the unique advantages of polymers in different whitening systems remain limited. A comprehensive understanding of both the active ingredients and delivery technologies is critical to balancing esthetic outcomes with long-term oral health. From a clinical perspective, polymer-based carriers might contribute to reducing whitening-related tooth sensitivity, improving patient comfort, and providing more predictable treatment outcomes. Continued research is needed to clarify optimal formulations and application protocols, ensuring safer and more effective tooth-whitening practices in both clinical and home-use scenarios. Full article