Search Results (167)

While many kinds of reactive compatibilizers (RCs) have been artificially created for reducing interfacial tension in immiscible polymer blends, the effect of RCs on co-continuity formation (preferred in application) remains controversial. In this work, we selected the previously reported poly(vinylene fluoride)/poly(L-lactic acid)/reactive comb compatibilizer (PVDF/PLLA/RCC) blend system as the model system, in which the reaction between epoxy groups in RCC and terminal carboxyl groups in PLLA upon blending can produce glycidyl methacrylate (GMA)-PLLA side chains located at the PVDF/PLLA interface. By manipulating PVDF/PLLA composition ratio and RCC content, a half-U-shaped co-continuous phase diagram with an upward opening was obtained, suggesting a promoting effect of RCC on PVDF/PLLA co-continuity. This can be attributed to both the high viscosity of PLLA/RCC and the inhibited PVDF phase coalescence. On the one hand, owing to the significantly increased viscosity of PLLA/RCC relative to neat PLLA, the decreased viscosity ratio of PVDF to PLLA(/RCC) can lower the co-continuous PVDF/PLLA composition ratio. On the other hand, the coalescence of PVDF phase in PVDF/PLLA/20%RCC can be effectively inhibited due to the addition of RCC, opposite to the inclined PLLA phase coalescence in the neat PVDF/PLLA blend with high PVDF fraction (e.g., 80%). Our results provide guidance for evaluating and selecting RCs for a specific immiscible polymer blend in practical application. Full article

(1) Background: Cerium silicate (CeSi) nanoparticles (NPs) have potential as a restorative filler particle with multifunctional properties to improve longevity. To increase the biological activity, these nanoparticles can be fabricated with ultrasmall pores (mesoporous) (MPCeSi-NP) that can be loaded with a polyphosphate inhibitor, such as gallein. (2) Methods: MPCeSi-NPs were custom-synthesized with a microemulsion method, using cetyltrimethylammonium bromide (CTAB) as a template for self-assembly. Biocompatibility with oral keratinocytes/fibroblasts was tested, with the addition of examining the biomineralization potential with human bone-marrow-derived mesenchymal stromal cells (BM-MSCs). MPCeSi-NP, loaded with gallein, was tested against Rothia dentocariosa (Rd). MPCeSi-NP was added to a resin matrix of triethylene glycol dimethacrylate (TEGDMA) and Bisphenol A-glycidyl methacrylate (BisGMA) with subsequent mechanical properties evaluation. (3) Results: MPCeSi-NPs had high biocompatibility with oral keratinocytes and fibroblasts, especially at concentrations below 300 µg/mL. MPCeSi-NPs induced the biomineralization of BM-MSCs. Higher cerium levels increased mineralization. MPCeSi-NP had weak antimicrobial activity against Rd. At 1% wt, MPCeSi-NPs did not reduce the polymerization potential and mechanical properties of a TEGDMA:BisGMA polymer material, with controlled release of gallein in a simulated degradation model. (4) Conclusions: MPCeSi-NPs are highly biocompatible and bioinductive and have the potential to improve the biological response of current restorative materials. Full article

Porous glycidyl methacrylate-based copolymers crosslinked with ethylene glycol dimethacrylate (EGDMA) and trimethylolpropane trimethacrylate (TMPTMA) were synthesized via suspension–emulsion polymerization and subsequently functionalized with triethylenetetramine. The effect of the monomer composition on the epoxy group content and porous structure was systematically investigated by varying the GMA-to-crosslinker molar ratio from 1:1 to 5:1. Increasing the GMA fraction enhanced the epoxy group content (2.8–5.0 mmol/g) but significantly reduced the specific surface area (333–23 m²/g), indicating a trade-off between functionality and porosity. ATR-FTIR and elemental analysis confirmed successful amine functionalization while preserving a considerable degree of porosity. The modified copolymers were evaluated for Cr(VI) removal, showing strong pH dependence, with maximum efficiency at pH 3 due to electrostatic interactions between protonated amine groups and HCrO₄⁻ ions. Equilibrium studies revealed saturation-type behavior, with a maximum sorption capacity of 165.47 mg/g for TMPTMA-based copolymers. Despite the higher nitrogen content in EGDMA-based materials, TMPTMA-crosslinked copolymers exhibited a superior adsorption performance, demonstrating that pore accessibility, rather than functional group density alone, governs adsorption efficiency. These findings provide insight into the rational design of amine-functionalized porous polymer sorbents for efficient chromium(VI) removal. Full article

Background/Objectives: Diabetic wound healing faces significant challenges due to the harsh microenvironment of wounds such as high blood glucose levels, excessive inflammation, persistent infection, upregulated reactive oxygen species (ROS), and damaged new blood vessels. Therefore, developing hydrogel dressings with microenvironmental regulation functions has become an important strategy in treating diabetic wounds. Methods: In this study, an ultraviolet in situ crosslinked hydrogel (D@H/E) was developed using methacrylic anhydride modified hyaluronic acid (HA-MA) and glycidyl methacrylate modified ε-polylysine (EPL-GMA), loaded with the iron chelating agent desferrioxamine (DFO). The physicochemical and biochemical properties of the hydrogel were comprehensively characterized, and its efficacy as a dressing for diabetic wounds was evaluated in a STZ-induced hyperglycemic mouse model. Results: This hydrogel demonstrated remarkable multidimensional effects by alleviating oxidative stress damage, inhibiting bacterial infection, regulating inflammatory responses, mitigating ferroptosis, and promoting cell migration and tubule formation. Specifically, the DFO-loaded hydrogel achieved a high DPPH radical scavenging efficiency of 80.8% and exhibited excellent antibacterial activity, with over 99.8% inhibition against both S. aureus and E. coli. In streptozotocin (STZ)-induced diabetic mice, the hydrogel accelerated wound closure to near completion by day 14. Mechanistically, it significantly upregulated CD206 expression to promote M2 macrophage polarization, upregulated the expression of angiogenesis-related factors to promote angiogenesis at the wound site, and enhanced GPX4 expression to alleviate ferroptosis. Conclusions: By orchestrating multi-dimensional synergy that combines ROS scavenging, infection control, immune regulation, and anti-ferroptosis, this D@H/E hydrogel system effectively remodels the harsh diabetic wound microenvironment, offering a promising platform for chronic wound management. Full article

This study investigates the key performance-related fuel properties of emulsifier–diesel solutions and ethanol-in-diesel microemulsions. This work begins with the in situ polymerization of long alkyl chain-substituted glycidyl methacrylate (R-GMA) in diesel and the optional presence of a second methacrylate monomer. The resulting diesel-soluble oligomer functions as a nonionic emulsifier. Controlled amounts of ethanol are subsequently incorporated into the emulsifier–diesel solution to form a stable microemulsion, referred to as E-Diesel. This study examines how the structure of the emulsifier influences key fuel properties, including (i) ethanol–diesel miscibility, (ii) gross calorific value, (iii) Ramsbottom carbon residue (% of fuel), (iv) entrapped polycyclic aromatic hydrocarbons (PAHs), and (v) fuel lubricity. Both the hydrophilic–hydrophobic balance and the structure of the emulsifier side chains are found to significantly affect these properties. Compared with neat diesel, oligomeric emulsifiers enable the substantial dispersion of ethanol in diesel (up to 18 wt.%). The resulting fuel exhibits a gross calorific value exceeding the theoretical sum of diesel and ethanol at the same composition (a synergistic effect) and achieves an enhancement in lubricity up to 49.5% relative to neat diesel at a 5% emulsifier loading. Although the presence of emulsifiers leads to an increase in the carbon residue by up to 54.7% compared to neat diesel during controlled pyrolysis, it simultaneously reduces the PAH content in the exhaust. Overall, this study establishes fundamental correlations among microemulsion stability, combustion synergy, carbon residue formulation, and fuel lubricity, which are governed by the structure of the emulsifier. Full article

Polyethylene terephthalate (PET) has become the predominant material for single-use packaging owing to its cost and performance advantages. However, massive post-consumer waste leads to environmental concerns, and recycled PET from thermomechanical processing followed by chain extension often suffers from low toughness and poor processability, restricting its use to low-value applications. In this study, halloysite nanotubes (HNTs) and ethylene–methyl acrylate–glycidyl methacrylate random terpolymer (E-MA-GMA) were melt-blended with recycled PET to examine their synergistic modification effects. The DSC results show that HNTs retain a nucleating effect on recycled PET even with the co-addition of E-MA-GMA, albeit with a substantial reduction compared with their effect when used alone. Nevertheless, rheological measurements indicate that the combined introduction of E-MA-GMA and HNTs imposes a significantly stronger restriction on the relaxation behavior of recycled PET molecular chains than the individual addition of either HNTs or E-MA-GMA. This is attributed to the interfacial reactions between E-MA-GMA and the recycled PET matrix, as well as between E-MA-GMA and HNTs, leading to the formation of branching and hybrid structures. This synergistic restraint markedly reduces the crystallization growth rate of PET. As a result, the recycled PET/E-MA-GMA/HNTs composites maintain relatively lower crystallinity compared with the recycled PET/E-MA-GMA composite after high-temperature injection molding or annealing treatment, leading to superior impact resistance. The impact strength of the recycled PET/E-MA-GMA/HNTs composites is 2.28 and 2.14 times that of the recycled PET/E-MA-GMA composite under high-mold-temperature injection molding and annealing conditions, respectively. The approach presented here facilitates the substitution of virgin plastics with recycled PET in demanding applications. Full article

Nanogels provide unique opportunities for stabilizing fragile enzymes through soft, hydrated polymer networks. Here, we report the development of a glutathione peroxidase (GPx)-loaded nanogel (GPxNG) engineered via a mild “grafting-to” epoxy–amine coupling strategy to enhance enzyme stability and antioxidant function. An amphiphilic copolymer composed of methacrylated 2,2,6,6-tetramethyl-4-piperidyl (PMA) and glycidyl methacrylate (GMA) was synthesized by controlled reversible addition–fragmentation chain-transfer (RAFT) polymerization using a poly(ethylene glycol) (PEG) macro-chain transfer agent (macro-CTA), yielding well-defined polymer chains with reactive epoxy groups. Covalent conjugation between polymer epoxides and GPx enzyme surface amines generated soft, PEGylated nanogels with high coupling efficiency, uniform particle sizes, and excellent colloidal stability. The engineered nanogels exhibited shear-thinning injectability, robust storage stability, and non-cytotoxic behavior in RAW 264.7 macrophages. Compared with native GPx enzyme, GPxNGs demonstrated significantly enhanced reactive oxygen species (ROS) scavenging activity, including strong inhibition of lipid peroxidation and copper-induced low-density lipoprotein (LDL) oxidation. Importantly, the nanogels preserved GPx enzyme activity after extended storage, freeze–thaw cycles, and repeated catalytic use, whereas the free enzyme rapidly lost function. This protective effect arises from the nanoscale confinement of the GPx enzyme within the flexible PEG-based network, which limits unfolding and aggregation. Overall, this work introduces a simple and biocompatible “grafting-to” nanogel platform capable of stabilizing redox-active enzymes without harsh conditions. The GPx nanogels combine high enzymatic preservation, potent antioxidant activity, and excellent handling properties, highlighting their potential as a therapeutic nanoplatform for mitigating oxidative stress-associated disorders such as atherosclerosis. Full article

This study aimed to assess how different resin matrix formulations affect the fatigue resistance of resin dental composites. Model dental composites were formulated using six distinct monomer mixtures: two Bis-GMA (bisphenol A-glycidyl methacrylate):TEGDMA (triethylene glycol dimethacrylate) (60:40 and 80:20 mole%), two UDMA (urethane dimethacrylate):TEGDMA (60:40 and 80:20 mole%), one Bis-GMA:UDMA:TEGDMA (35:35:30 mole%), and one Fit852:UDMA:TEGDMA (35:35:30 mole%). Cyclic fatigue resistance (CFR) of the resin composites was measured in a biaxial test mode using staircase analysis. Additional evaluations included biaxial flexural strength (BFS), degree of conversion (DC), water sorption (WS), and viscoelastic properties of the unfilled resins, such as the storage modulus (E′), loss modulus (E″), tan δ (E″/E′), and stiffness (k′). Data were subjected to one-way ANOVA with Tukey post hoc analyses. Pearson correlation and stepwise regression analyses were conducted to examine the relationships among variables. The UT6040 model composite exhibited the highest CFR (82.61 ± 8.83 MPa), significantly outperforming other formulations. Tan δ of the resin matrix showed the strongest correlation with CFR (r = 0.974), and was also shown to be the most influential predictor for the CFR of the particulate composites. The composition of the resin matrix has a significant impact on the CFR of dental composites. Among the properties evaluated, the viscoelastic parameter tan δ emerged as a strong and reliable predictor of CFR, emphasizing the importance of targeting viscoelastic behavior in the design of dental composite formulations. Full article

The production of polymer nanocomposites from supertough blends reinforced with carbon-based nanofillers has garnered attention in recent years due to improvements in their mechanical, thermal, and electrical properties. Currently, the main challenge is to develop materials with balanced performance for diverse industrial demands. In this context, this work aimed to produce nanocomposites of poly(butylene terephthalate) (PBT) and poly(ethylene-octene) grafted with glycidyl methacrylate (POE-g-GMA), reinforced with carbon nanotubes (MWCNTs). The PBT, the PBT/POE-g-GMA blend, and the respective MWCNT nanocomposites were initially premixed in an internal mixer and then processed in a co-rotational twin-screw extruder. After processing, they were injection-molded to obtain tensile, impact, and HDT test specimens. Mechanical (tensile, impact, and Shore D hardness), thermal (differential scanning calorimetry—DSC), thermomechanical (heat deflection temperature—HDT), electrical resistivity/conductivity, morphology, and Fourier transform infrared spectroscopy (FTIR) properties were evaluated. The results demonstrated a good balance among the investigated properties, with improvements in mechanical, thermal, and thermomechanical properties when compared to PBT. The impact strength of the nanocomposites reached 186 J/m, approximately 158% higher than that of neat PBT. The HDT reached approximately 55 °C in the PBT/POE-g-GMA/MWCNT5 nanocomposites, while the crystallization temperature increased by 11 °C, as evidenced by DSC, an aspect of great relevance for industrial applications. Furthermore, the PBT/POE-g-GMA/MWCNT5 nanocomposites exhibited an electrical conductivity of 1.06 × 10⁻⁷ S/cm, indicating potential for electrical applications. Full article

Phytic acid, as a natural originated compound with multi phosphate side groups, is known to increase the corrosion protection and thermal resistance of the coatings. In this study, two different acrylic emulsion polymers containing epoxy and silane reactive functional groups (glycidyl methacrylate (GMA) and vinyltriethoxysilane (VTES)) were synthesized via emulsion polymerization and mixed with phytic acid (PA) solution in different ratios (5, 10, 15 wt%) for use as binders in leather finishing applications. The colloidal stability, particle size distribution, and chemical structures of the synthesized polymers were characterized through comprehensive analyses. The resulting reactive copolymer dispersions were used as binders in finishing formulations and applied to crust shoe upper leathers The coating performance was evaluated in terms of rub fastness, flex resistance, water spotting, and thermal resistance, using the unmodified reactive acrylic binders (G0 and V0) as reference systems to assess the improvements achieved. Both phytic acid-modified binders exhibited strong film integrity and maintained high dry rub fastness up to 2000 cycles and wet rub fastness up to 250 cycles at phytic acid concentrations of 5–10 wt%. Increasing the phytic acid content beyond this range led to reduced dispersion stability and partial loss of coating performance. The results confirm that incorporating moderate levels of phytic acid into reactive acrylic emulsions enhances coating durability and thermal resistance without compromising film appearance, offering a safer and more sustainable alternative to conventional crosslinking systems for leather finishing applications. Full article

The growing demand for sustainable solutions in the plastics industry has highlighted the need to reintroduce post-industrial polymer waste into high-performance applications. This study focuses on the mechanical recycling of automotive scraps containing variable proportions of polycarbonate (PC), acrylonitrile–butadiene–styrene (ABS), and a commercial PC/ABS blend. After determining the composition of two representative batches, a screening of seven commercial compatibilizers and impact modifiers was performed to improve impact strength. Among them, an ethylene–methyl acrylate–glycidyl methacrylate (E-MA-GMA) terpolymer was identified as the most effective additive. Its influence was further investigated through a mixture design approach, varying the composition of the three polymer phases and the additive content (0–10 wt.%). The resulting response surface model revealed a significant increase in impact resistance in PC-rich formulations with increasing E-MA-GMA content, while ABS and PC/ABS showed more complex trends. Rheological, mechanical, and thermal analyses supported the observed behavior, suggesting improved matrix compatibility and reduced degradation during processing. The proposed model enables the prediction of impact performance across a wide range of compositions, offering a practical tool for the optimization of recycled blends. These findings support the potential of targeted compatibilization strategies for closed-loop recycling in the automotive sector. Full article

This study explored the feasibility of using a plastic vacuum chamber for the Filament-Assisted Chemical Vapor Deposition (FACVD) of polymer thin films. Traditional chemical vapor deposition (CVD) methods often require high vacuum and elevated temperatures, which limit their use for heat-sensitive and flexible substrates. FACVD enables polymer deposition under mild vacuum and temperature conditions, providing an opportunity to utilize plastic vacuum chambers as cost-effective and easily machinable alternatives to metallic chambers. In this study, a custom-designed acrylic chamber was fabricated and integrated into an FACVD system. Glycidyl methacrylate (GMA) and tert-butyl peroxide (TBPO) were considered as the monomer and initiator, respectively, for creating thin films under a low-temperature and moderate-vacuum deposition process. Polymeric film (pGMA) contains reactive epoxy groups that allow versatile post-polymerization modifications and are widely applied in coatings and biomedical fields. Preliminary experiments demonstrated the successful growth of pGMA thin films, with Fourier-transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS) confirming the characteristic polymer features, including the disappearance of the C=C stretching band as direct evidence of polymerization. Ellipsometry determines a uniformity of film thickness of approximately 85% for the 4-inch wafers’ area, with deposition rates in the range of 18–26 nm/h. These results highlight the potential of polymer-based chambers as cost-effective and versatile alternatives to advanced vapor-phase polymerization processes. Full article

This work aims to design versatile hybrids fabricated by poly(hydroxypropyl methacrylate-co-glycidyl methacrylate) gels loaded with pristine montmorillonite, P(HPMA-co-GMA)/Mmt, by varying the clay content. Insights into design of epoxy-functional hybrids were provided by combining in situ copolymerization reactions with solution mixing to evaluate the effect of aluminosilicate addition on structure–property changes in (alkyl)methacrylate-based gels. Comprehensive analyses were conducted regarding the composition and structural properties of hybrids in the presence of Mmt. The hybrids exhibited excellent swelling, salt surfactant tolerance, and pH sensitivity depending on the composition. The higher the Mmt concentration, the lower the swelling ratio; however, the compressive moduli did not change monotonically with increasing Mmt from 0.80 to 2.20% (w/v). Dye adsorption revealed the effects of variables (dye type, pH, contact time, concentration) on adsorptive properties of hybrids towards cationic methylene blue (MB) and anionic sunset yellow, allura red, blue brilliant, carmoisine, and tartrazine dyes. Adsorption kinetics of MB obeyed pseudo-second-order model, and the maximum dye adsorption capacity for hybrids increased from 5.01 mg g⁻¹ to 16.42 mg g⁻¹, while adsorption isotherms were defined by the Freundlich model. The proposed hybrids have emerged as alternative materials that enable multiple uses of same adsorbent for the removal of different types of pollutants. Full article

Growing concerns over the toxicity and sustainability of dental materials have driven the search for alternatives to bisphenol A-glycidyl methacrylate (Bis-GMA), a widely used dental resin monomer associated with health risks. This study highlights the potential of less health-hazardous dental formulations by incorporating high-value materials derived from the glycolysis of poly(ethylene terephthalate) (PET). Dimethacrylated oligoesters (PET-GLY-DM), synthesized through the methacrylation of PET glycolysis products, were blended with Bis-GMA and triethylene glycol dimethacrylate (TEGDMA), toward the gradual replacement of Bis-GMA content. The innovative PET-GLY-DM-based resins exhibited a higher degree of conversion compared to traditional Bis-GMA/TEGDMA formulations, as measured by FTIR spectroscopy, accompanied by an increase in polymerization shrinkage, evaluated via a linear variable displacement transducer system. While the incorporation of PET-GLY-DM slightly reduced flexural strength and elastic modulus, it significantly decreased water sorption, resulting in a smaller reduction in mechanical properties after water immersion for 7 days at 37 °C and improved long-term performance. Furthermore, PET-GLY-DM resins exhibited low bisphenol-A (BPA) release measured with HPLC. It was thus confirmed that PET-GLY-DM resins derived from the glycolysis of PET wastes represent a promising alternative to conventional light-cured dental resins, offering reduced BPA release and improved water resistance. Full article

Biodegradable polymers offer environmental advantages compared to fossil-based alternatives, but they currently lack the stretchability required for demanding applications such as mesh fabrics for woven flexible intermediate bulk container (FIBC) bags and stretch, shrink, and cling films. The goal of this research is to enhance the stretchability of biodegradable blends based on 80% poly(butylene adipate-co-terephthalate) (PBAT) and 20% poly(lactic acid) (PLA) through reactive extrusion. Radical initiator (dicumyl peroxide (DCP)) and chain extenders (maleic anhydride (MA), glycidyl methacrylate (GMA)) were employed to improve the melt strength and elasticity of the extruded films. The reactive blends were initially prepared using a batch mixer and subsequently compounded in a twin-screw extruder. Films were produced via cast extrusion. 0.1% wt. DCP led to a 200% increase in elongation at break and a 44% improvement in tensile strength. Differential scanning calorimetry and scanning electron microscopy revealed enhanced miscibility between components. Shear and complex viscosity increased by 38% and 85%, compared to the neat blend, respectively. Reactive extrusion led to a better dispersion and distribution of the phases. An improved interfacial adhesion between the phases, in addition to higher molecular weight, led to enhanced melt strength and improved stretchability. Full article