Search Results (265)

This study explored the formation of soft colloidal particles from a diblock ionomer (DI) with the monomeric composition (acrylonitrile)_x-co-(glycidyl methacrylate)_y-b-(3-sulfopropyl methacrylate potassium)_z—abbreviated as (A_xG_y)S_z, where x >> z > y. A colloidal dispersion was generated by introducing water into the pre-prepared DMSO solutions of DI, which led to micelle formation and subsequent coagulation. The assembly of the hydrophobic (A_xG_y) blocks was influenced by water content and chain conformational flexibility (the ability to adopt various forms of conformation). The resulting microgel structure (in particle form) consists of coagulated micelles characterized by discrete internal hydrophobic gel domains and continuous external hydrophilic gel layers. Characterization methods included light scattering, zeta potential analysis, and particle size distribution measurements. In contrast, the copolymer (A_xG_y) chains form random coil aggregates in DMSO–H₂O mixtures, displaying a chain packing state distinct from the hydrophobic gel domains as aforementioned. Additionally, the amphiphilic glycidyl methacrylate (G) units within the (A_xG_y) block were found to modulate the microgel dimensions. Notably, the nanoscale hydrogel corona exhibits high accessibility to reactive species in aqueous media. The typical microgel has a spherical shape with a diameter ranging from 50 to 120 nm. It exhibits a zeta potential of −65 mV in a neutral aqueous medium; however, it may precipitate if the metastable colloidal dispersion state cannot be maintained. Its properties could be tailored through adjusting the internal chain conformation, highlighting its potential for diverse applications. Full article

3D printing with biodegradable polymers such as polylactic acid (PLA) is a sustainable alternative to conventional petroleum-derived plastics. However, improving the mechanical properties of PLA remains a challenge. This study explores the incorporation of chemically treated hemp fibers to improve the interfacial adhesion and mechanical strength of PLA filaments. Samples with PLA and hemp were prepared by subjecting the fibers to cationization treatment with (3-chloro-hydroxypropyl) tri-methylammonium (EPTA) and functionalization with glycidyl methacrylate (GMA). EPTA improves adhesion mainly through surface modification, increasing reactive functional groups in cellulose, while GMA improves interfacial adhesion by forming covalent bonds with both the fiber and PLA and improves the dispersion of the fiber in the matrix. Mechanical properties were evaluated by tensile testing, as well as fracture morphology by scanning electron microscopy (SEM) and X-ray energy dispersive analysis (EDS). The results showed that the addition of untreated hemp significantly reduced the strength of PLA, but cationization with EPTA improved interfacial adhesion and increased tensile strength by 615%. The combination of treated fibers and GMA further optimized the mechanical properties, reaching values similar to pure PLA. These findings indicate that the chemical modification of natural fibers facilitates their integration into PLA filaments for 3D printing, promoting sustainable materials without compromising mechanical performance. Full article

The printing precision of hydrogels directly determines the mechanical and electrical performance of scaffolds. In this study, poly(3,4-ethylenedioxythiophene)-poly (styrenesulfonate) (PEDOT:PSS) was directly compounded with glycidyl methacrylate-modified silk fibroin (Sil-MA) through a one-pot method to increase the solid content of the printing ink, enhancing its mechanical, electrical, and printability properties. A dual-network photo-curable conductive silk fibroin composite hydrogel (CDMA) was successfully prepared. The results show that the introduction of PEDOT:PSS significantly improved the conductivity of the hydrogel. (The bandgap decreased from 2.36 eV to 1.125 eV, and the maximum conductivity reached 0.534 S/m.) It also enhanced the microscopic 3D network density and mechanical properties of the hydrogel (compressive modulus up to 192 kPa). Moreover, the hydrogel demonstrated good stability during cyclic stability testing, providing a new approach to developing materials capable of high-precision printing with stable electrical performance. Full article

In this study, we developed a novel one-pot synthesis method to fabricate well-defined single-chain polymeric nanoparticles (SCNPs) integrated with interpenetrating polymer network (IPN) systems. The synthesis process involved an initial intramolecular crosslinking of poly(methyl methacrylate-co-glycidyl methacrylate) to form SCNP followed by intermolecular crosslinking to produce single-chain nanogel (SCNG) structures. In addition, the achieved single-chain polymeric nanoparticle was subsequently incorporated into an IPN structure through urethane bond formation and a Diels–Alder click reaction involving furfuryl methacrylate (FMA) and bismaleimide (BMI). The thermal properties, swelling behaviors, and morphologies of the resulting SCNP-IPN systems were investigated. This work presents a novel strategy that integrates the single-chain folding concept with IPN systems, providing a promising platform for the development of robust and functional polymeric materials with potential applications in advanced materials science. Full article

This paper describes the synthesis of a viscosity-reducing agent using butyl acrylate (BA), ethyl methacrylate (EMA), acrylic acid (AA) and N-hydroxymethylacrylamide (N-MAM) monomers through emulsion polymerization. A series of viscosity-reducing agents were developed by incorporating varying amounts of glycidyl methacrylate (GMA) monomers. The reaction mechanism of epoxy acrylate viscosity reducer was analyzed by Fourier transform infrared spectroscopy (FTIR). Additionally, the particle size and Zeta potential were used to analyze the stability of the polymer and the difference in the polymer after adding GMA monomer. Thermogravimetric (TG) analysis indicated a significant improvement in the thermal stability of the resin due to GMA modification. The viscosity reduction test results demonstrated a substantial decrease in the viscosity of heavy oil, along with a notable increase in the viscosity reduction rate. The FTIR analysis results confirmed that GMA successfully introduced polyacrylate molecular chains. Furthermore, particle size and Zeta potential measurements showed that the average particle size of the emulsion increased from 132 nm to 187 nm, while the Zeta potential changed from −43 mV to −40 mV with the addition of 15% GMA. Compared with W0, the final thermal degradation temperature of W15 increased from 450 °C to 517 °C. When the GMA content reached 15 wt%, the maximum weight loss temperature increased by approximately 12 °C compared to the sample without GMA. Specifically, adding 8% W15 epoxy acrylate resulted in an 89% viscosity reduction rate for heavy oil, demonstrating an excellent viscosity reduction effect. This study successfully developed a novel epoxy acrylate viscosity reducer using a simple synthesis method, showcasing excellent stability, cost-effectiveness and remarkable viscosity reduction. Full article

Biomedical cotton gauzes (C0), after a first functionalization with glycidyl methacrylate (GMA) by a Fenton’s reaction (material C1), can be further modified in order to make them suitable for the adsorption and next release of drugs. Indeed, either after opening the epoxide ring through the addition of water (material C2) or after the introduction of amino groups through reaction with diamines (1,2-diaminoethane (material C3), 1,6-diaminohexane (material C4) and 1,12-diaminododecane (material C5)), the new gauzes can be uploaded with drugs. Both ibuprofen (IB), a non-steroidal anti-inflammatory, and amoxicillin (AM), a wide-spectrum β-lactam antibiotic, are efficiently adsorbed from their aqueous solutions at 20 °C onto C2–C5 (up to ≈0.8 mmol g⁻¹ for IB and up to 0.4 mmol g⁻¹ for AM) but not onto C0 and C1. The release of both IB and AM is affected by the ionic strength of the medium in which the release takes place. Indeed, kinetic experiments conducted with a physiological solution (NaCl (aq, 0.9% w/v) showed good release efficiencies while only modest or negligible release was observed if deionised water was the release medium. Moreover, the kind of functionalization plays an important role during both the adsorption and the release. The gauzes C3–C5 can be uploaded with a higher amount of drug relative to C2. Conversely, the drug is released quickly and in a higher amount from C2 relative to the gauzes containing the amino groups. Full article

This study presents the formulation and comprehensive characterization of compatibilized polyamide 6 (PA6)/cyclic olefin copolymer (COC) blends with the aim of developing a self-healing matrix for thermoplastic structural composites. Rheological analysis highlighted the compatibilizing effect of ethylene glycidyl methacrylate (E-GMA), as evidenced by an increase in viscosity, melt strength (MS), and breaking stretching ratio (BSR), thus improving the processability during film extrusion. E-GMA also decreased COC domain size and improved the interfacial interaction with PA6, which was at the basis of a higher tensile strength and strain at break compared to neat PA6/COC blends. E-GMA also significantly boosted the healing efficiency (HE), measured via fracture toughness tests in quasi-static and impact conditions. The optimal healing temperature was identified as 160 °C, associated with an HE of 38% in quasi-static mode and 82% in impact mode for the PA6/COC blends with an E-GMA content of 5 wt% (PA6COC_5E-GMA). The higher healing efficiency under impact conditions was attributed to the planar fracture surface, which facilitated the flow of the healing agent in the crack zone, as proven by fractography analysis. This work demonstrates the potential of E-GMA in fine-tuning the thermomechanical properties of PA6/COC blends. PA6COC_5E-GMA emerged as the formulation with the best balance between processability and self-healing efficiency, paving the way for advanced multifunctional self-healing thermoplastic composites for structural applications. Full article

This study was conducted to evaluate the material properties of polymer-infiltrated zinc oxide networks (PICN) and the effect of using a phosphate monomer-containing primer applied before polymer infiltration. A total of 148 ZnO-network (zinc oxide) specimens were produced: n = 74 were treated with a primer before polymer infiltration and light curing, while the remaining specimens were untreated. Each group was divided into two subgroups (n = 37) based on the infiltrating polymer: UDMA (aliphatic urethane-dimethacrylates)-TEGDMA (triethylene glycol-dimethacrylate) or BisGMA (bisphenol A-glycidyl-methacrylate)-TEGDMA. Additionally, n = 7 specimens of each polymer type were prepared for comparison. Then, biaxial flexural strength was measured before and after 150 days of water storage at 37 °C, including 37,500 thermal cycles (5 °C to 55 °C). The Vickers hardness, surface roughness, and water absorption at 37 °C were also tested. The initial biaxial flexural strength was reduced in the ZnO network specimens compared to in the pure polymers. Primer application improved the flexural strength, though the strength of BisGMA-TEGDMA significantly decreased after water storage. The ZnO network increased hardness, and the polymer-infiltrated networks showed higher roughness post-grinding and absorbed less water than the pure polymer groups. The ZnO networks did not improve the flexural strength over that of the pure polymers. However, the primer’s positive impact and the network’s long-term stability suggest potential if the network structure can be modified to contain thicker, more stable branches. Full article

The packaging industry has made efforts to reduce food waste and improve the resilience of food systems worldwide. Active food packaging, which incorporates active agents, represents a dynamic area where industry and academia have developed new strategies to produce innovative and sustainable packaging solutions that are more compatible with conventional options. Due to health and environmental concerns, industries have sought alternatives to petroleum-based materials and have found biopolymers to be a viable option because of their biodegradable and safe nature. The combination of PLA/TPS has emerged as an effective system for packaging film; however, they are thermodynamically immiscible. This work highlights the development of a starch-based compatibilizer to connect the PLA and TPS phases by functionalizing maize starch with glycidyl methacrylate, glycerol, or garlic oil. Garlic oil was chosen for its plasticizing ability and antioxidant properties. The films produced exhibited excellent compatibility, with enhanced interfacial adhesion between PLA and TPS components. The introduction of compatibilizers also increased the systems’ crystallinity and improved their mechanical properties. The wettability of the films significantly increased with higher garlic oil content, along with enhanced antioxidant properties. These advancements will enable the production of a compatible PLA/TPS system with improved properties for application in the packaging industry. Full article

Cross-linked polyethylene (XLPE) is applied in most advanced high-voltage direct-current (HVDC) power cable insulations, which are produced via dicumyl peroxide (DCP) technology. The electrical conductivity of insulation material can be increased by cross-linking byproducts from the DCP process. Hence, currently much attention is being paid to a new process to produce cross-linking byproduct-free XLPE. The cross-linking in situ between ethylene–glycidyl methacrylate copolymer and 1,5-disubtituted pentane via reactive compounding is a substitute for DCP. The reaction potential energy information of the eighteen reaction channels was obtained at the B3LYP/6-311+G(d,p) level. Results demonstrated that epoxy groups and 1,5-disubtituted reactive groups can react in situ to realize the XLPE-based network structure via covalent linking, and epoxy ring openings yielded ester. 1,5-disubtituted pentane played a cross-linker role. The reactivity of the carboxyl group was stronger than that of the sulfydryl or hydroxyl group. The reaction channel RTS1 was more kinetically favorable due to the lower reaction Gibbs energy barrier height of 1.95 eV. The cross-linking network construction of the new XLPE insulation without byproducts opens up the possibility of DCP substitution, which is beneficial to furthering the design of thermoplastic insulation materials for power cables in the future. Full article

Infrared (IR) radiation curing technology has a high potential to improve the curing process of thermosetting polymers. To investigate the IR curing reaction mechanism, the present study explores the curing kinetics of glycidyl methacrylate (GMA)/dodecanedioic acid (DDDA) powder coatings subjected to IR radiation. Fourier-transformed infrared (FT-IR) spectroscopy is employed to record the concentration of epoxide groups with respect to time under different temperature conditions, with the reaction conducted under IR radiation. The resulting data are then fitted by the Levenberg–Marquardt algorithm using MATLAB software to obtain the kinetic parameters, namely the rate constant (k), catalytic constants (n, m), manifestation activation energy (E), and the pre-exponential factor (A) of the curing reaction. Additionally, this study proposes a new concept: the ‘photo-thermal synergistic effect’ of infrared curing and its evaluation criteria using a dimensionless quantity. Incredibly, this index integrates the impact of IR curing technology on two aspects: the curing process and the properties of the cured product. Overall, this study deepens our understanding of the IR curing reaction mechanism and provides a reference for the application of this technology in practical engineering. Full article

In the last decade, the task of developing environmentally friendly and cost-effective methods for obtaining stable superhydrophobic coatings has become topical. In this study, we examined the effect of the concentrations of filler and polymer binder on the hydrophobic properties and surface roughness of composite coatings made from organic–aqueous compositions based on hexyl methacrylate (HMA) and glycidyl methacrylate (GMA) copolymers. Silicon dioxide nanoparticles were used as a filler. A single-stage “all-in-one” aerosol application method was used to form the coatings without additional intermediate steps for attaching the adhesive layer or texturing the substrate surface, as well as pre-modification of the surface of filler nanoparticles. As the ratio of the mass fraction of polymer binder (Wn) to filler (Wp) increases, the coatings show the lowest roll-off angles among the whole range of samples studied. Coatings with an optimal mass fraction ratio (Wn/Wp = 1.2 ÷ 1.6) of the filler to polymer binder maintained superhydrophobic properties for 24 h in contact with a drop of water in a chamber saturated with water vapor and exhibited roll-off angles of 6.1° ± 1°. Full article

This study is aimed at developing a fibre-reinforced polymer composite with a high bio-based content and to investigate its mechanical properties. A novel basalt fibre-reinforced polymer (BFRP) composite with bio-based matrix modified with different contents of star-like n-butyl methacrylate (n-BMA) block glycidyl methacrylate (GMA) copolymer has been developed. n-BMA blocks have flexible butyl units, while the epoxide group of GMA makes it miscible with the epoxy resin and is involved in the crosslinking network. The effect of the star-like polymer on the rheological behaviour of the epoxy was studied. The viscosity of the epoxy increased with increase in star-like polymer content. Tensile tests showed no noteworthy influence of star-like polymer on tensile properties. The addition of 0.5 wt.% star-like polymer increased the glass transition temperature by 8.2 °C. Mode-I interlaminar fracture toughness and low-velocity impact tests were performed on star-like polymer-modified BFRP laminates, where interfacial adhesion and impact energy capabilities were observed. Interlaminar fracture toughness improved by 45% and energy absorption capability increased threefold for BFRP laminates modified with 1 wt.% of star-like polymer when compared to unmodified BFRP laminates. This improvement could be attributed to the increase in ductility of the matrix on the addition of the star-like polymer, increasing resistance to impact and damage. Furthermore, scanning electron microscopy confirmed that with increase in star-like polymer content, the interfacial adhesion between the matrix and fibres improves. Full article

In this study, specific additives were incorporated in polyhydroxyalcanoate (PHB) and polylactic acid (PLA) blend to improve its compatibility, and so enhance the cell metabolic activity of scaffolds for tissue engineering. The formulations were manufactured through material extrusion (MEX) additive manufacturing (AM) technology. As additives, petroleum-based poly(ethylene) with glicidyl metacrylate (EGM) and methyl acrylate-co-glycidyl methacrylate (EMAG); poly(styrene-co-maleic anhydride) copolymer (Xibond); and bio-based epoxidized linseed oil (ELO) were used. On one hand, standard geometries manufactured were assessed to evaluate the compatibilizing effect. The additives improved the compatibility of PHB/PLA blend, highlighting the effect of EMAG and ELO in ductile properties. The processability was also enhanced for the decrease in melt temperature as well as the improvement of thermal stability. On the other hand, manufactured scaffolds were evaluated for the purpose of bone regeneration. The mean pore size and porosity exhibited values between 675 and 718 μm and 50 and 53%, respectively. According to the results, the compression stress was higher (11–13 MPa) than the required for trabecular bones (5–10 MPa). The best results in cell metabolic activity were obtained by incorporating ELO and Xibond due to the decrease in water contact angle, showing a stable cell attachment after 7 days of culture as observed in SEM. Full article

Oriented antibody immobilization has been widely employed in immunoassays and immunodiagnoses due to its efficacy in identifying target antigens. Herein, a heptapeptide ligand, HWRGWVC (HC7), was coupled to poly(glycidyl methacrylate) (PGMA) nanospheres (PGMA-HC7). The antibody immobilization behavior and antigen recognition performance were investigated and compared with those on PGMA nanospheres by nonspecific adsorption and covalent coupling via carbodiimide chemistry. The antibodies tested included bovine, rabbit, and human immunoglobulin G (IgG), while the antigens included horseradish peroxidase (HRP) and β-2-Microglobulin (β2-MG). The nanospheres were characterized using zeta potential and particle size analyzers, scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, and reversed-phase chromatography, proving each synthesis step was succeeded. Isothermal titration calorimetry assay demonstrated the strong affinity interaction between IgG and PGMA-HC7. Notably, PGMA-HC7 achieved rapid and extremely high IgG adsorption capacity (~3 mg/mg) within 5 min via a specific recognition via HC7 without nonspecific interactions. Moreover, the activities of immobilized anti-HRP and anti-β2-MG antibodies obtained via affinity binding were 1.5-fold and 2-fold higher than those of their covalent coupling counterparts. Further, the oriented-immobilized anti-β2-MG antibody on PGMA-HC7 exhibited excellent performance in antigen recognition with a linear detection range of 0–5.3 μg/mL, proving its great potential in immunoassay applications. Full article