Search Results (30)

Microplastic (MP) analysis in various environmental media currently faces significant challenges due to the complex and transportable nature of these materials. This study employed Fourier-transform infrared spectroscopy (FTIR) to investigate the presence of MPs in caddisfly larval cases, which incorporate vegetative fragments, sediment grains, and MP particles as building materials. The analysis of MPs in 2049 caddisfly larval cases revealed a total of 7553 items, resulting in an average of 3.7 items/case. The lowest recorded rate was 0.8 items/case, while the highest reached 18.2 items/case. Fiber MPs comprised 39.2% of the total, followed by fragment MPs at 30.8% and spherical MPs at 30%. Among the colors analyzed, blue MPs were the most prevalent, accounting for 36.6%, with white/transparent MPs at 22.1% and red MPs at 14.1%. MPs smaller than 100 µm were the most common, accounting for 37%, followed by MPs in the 100–250 µm range at 23.9%, larger than 500 µm at 22.3%, and those between 250 and 500 µm at 15.8%. Cellulose acetate was discovered to be the most abundant MP among different polymer types, followed by cellulose acetate butyrate, polyethylene terephthalate, poly(vinyl propionate), poly(ethylene glycol), poly(acrylonitrile-co-butadiene), cellulose propionate, hydroxyethyl cellulose, polyvinyl alcohol, glycerol triacetate, polystyrene, and poly(propylene glycol) methacrylate. These findings show the existence of MP in biotic components of these ecosystems, which has implications for aquatic biota health and freshwater quality, particularly in places influenced by human activity. Full article

The development of antimicrobial and antioxidant packaging materials is critical for improving food safety and extending shelf life. This study aimed to design and characterize low-density polyethylene (LDPE) and poly(ethylene-co-vinyl acetate) (EVA) films incorporating organically modified montmorillonite (OMt) nanocarriers loaded with carvacrol (C) and thymol (T) essential oil components. The incorporation of carvacrol and thymol into OMt was conducted through an evaporation/adsorption method without the use of organic solvents. In the next step, LDPE, EVA and OMtC or OMtT were melt-compounded in order to obtain films. Characterization of the bioactive nanocarriers and films was performed through X-ray diffraction (XRD), tensile testing, oxygen permeability measurements (OTR) and antioxidant assays. Films LDPE/EVA/OMtC and LDPE/EVA/OMtT showed improved mechanical strength and antioxidant activity, with IC₅₀ values between 0.32 and 0.52 mg/mL. Film with component weight ratio LDPE/EVA/OMtC equal to 80/10/10 also demonstrated enhanced barrier properties and significantly inhibited fungal growth on baguette bread for up to 60 days. These findings highlight the potential of these bioactive films to improve the microbial safety and shelf life of bakery products. Full article

Poly(ethylene-co-vinyl acetate) (PEVAc) is a copolymer that consists of non-polar polyethylene (PE) and a polar polyvinyl acetate (PVAc) monomer. PEVAc has high elasticity and is resilient, making it suitable for a variety of applications. However, the tensile strength of this copolymer needs to be improved for specific applications that require enough strength to tolerate high external tension or stress. This study proposed the use of dual-functionalized dolomite nanoparticles (DF-DNPs) composed of polar and non-polar nano-dolomite (P-DNPs and NP-DNPs) as nanofillers to reinforce the PEVAc. PEVAc/DF-DNP film appears to have a more homogeneous mixture, which is better for forming an optimal nanocomposite material. It also exhibits the highest tensile strength (10.48 MPa), elongation at break (1175.73%), and tensile toughness (62.12 MPa), which are higher by increments of 46.8%, 9.4%, and 20.3%, respectively, as compared to the neat PEVAc. The result proved that using DF-DNPs as a nanofiller can improve the strength of PEVAc while maintaining its flexibility to avoid brittleness of the nanocomposite film. Furthermore, its thermal characteristics were also successfully enhanced. A biostability assessment showed that the use of DF-DNPs as nanofiller caused the PEVAc copolymer to achieve the best water resistance, as it only exhibited a 2.63% weight increase, the lowest reduction in tensile properties among the studied fillers, and the best retention in surface degradation upon 3-month exposure to the in vitro environment. These findings indicate that the DF-DNPs help in developing a homogeneous nanocomposite by interacting with PE and PVAc. Full article

The impact of the anthropic activities in Antarctica is a concerning issue. According to the Scientific Committee on Antarctic Research, attention has to be paid to the next-generation contaminants deriving from both long-range atmospheric transport and local sources. In this study, the capabilities of transmission electron microscopy with energy-dispersive X-ray spectroscopy and Raman micro-spectroscopy were exploited to evaluate the size, morphology, and chemical composition of small micro- and nanoparticles, as well as their aggregates, in surface snow samples collected during the 2020–2021 austral summer in the coastal area of Victoria Land near the Mario Zucchelli research station. The presence of biological particles, mineral dust, sea salts, and small carbonaceous and plastic micro- and nanoparticles was assessed. Sulfate, carbonate, and nitrate minerals were detected in all the samples, whereas polyethylene, poly(ethylene-co-vinyl-acetate), and different kinds of carbonaceous materials were predominantly identified in the samples closest to the research base. The presence of small micro- and nanoparticles containing heavy metals and plastic polymers in samples collected in the areas surrounding the Italian research base highlights the impact of anthropogenic activities on the polar environment, suggesting the need for continuous monitoring to evaluate possible threats to the delicate Antarctic ecosystem. Full article

Movements in plants, such as the coiling of tendrils in climbing plants, have been studied as inspiration for coiling actuators in robotics. A promising approach to mimic this behavior is the use of multimaterial systems that show different elastic moduli. Here, we report on the development of magnetically controllable/triggerable multimaterial fibers (MMFs) as artificial tendrils, which can reversibly coil and uncoil on stimulation from an alternating magnetic field. These MMFs are based on deformed shape-memory fibers with poly[ethylene-co-(vinyl acetate)] (PEVA) as their core and a silicone-based soft elastomeric magnetic nanocomposite shell. The core fiber provides a temperature-dependent expansion/contraction that propagates the coiling of the MMF, while the shell enables inductive heating to actuate the movements in these MMFs. Composites with mNP weight content ≥ 15 wt% were required to achieve heating suitable to initiate movement. The MMFs coil upon application of the magnetic field, in which a degree of coiling N = 0.8 ± 0.2 was achieved. Cooling upon switching OFF the magnetic field reversed some of the coiling, giving a reversible change in coiling ∆n = 2 ± 0.5. These MMFs allow magnetically controlled remote and reversible actuation in artificial (soft) plant-like tendrils, and are envisioned as fiber actuators in future robotics applications. Full article

Aliphatic and aromatic polyesters of hydroxycarboxylic acids are characterized not only by biodegradability, but also by biocompatibility and inertness, which makes them suitable for use in different applications. Polyesters with high enzymatic hydrolysis capacity include poly(lactic acid), poly(ε-caprolactone), poly(butylene succinate) and poly(butylene adipate-co-terephthalate), poly(butylene succinate-co-adipate). At the same time, poly(lactic acid) is the most durable, widespread, and cheap polyester from this series. However, it has a number of drawbacks, such as high brittleness, narrow temperature-viscosity processing range, and limited biodegradability. Three main approaches are known for poly(lactic acid) modification: incorporation of dispersed particles or low molecular weight and oligomeric substances, copolymerization with other polymers, and blending with other polymers. The review includes an analysis of experimental works devoted to developing mixtures based on poly(lactic acid) and other polymers. Regularities in the formation of the structure of such systems and the possibility of controlling the properties of poly(lactic acid) are considered. Full article

Dielectrophoresis has recently been used for developing high performance elastomer-based structured piezoelectric composites. However, no study has yet focused on the development of aligned thermoplastic-based piezocomposites. In this work, highly anisotropic thermoplastic composites, with high piezoelectric sensitivity, are created. Molten-state dielectrophoresis is introduced as an effective manufacturing pathway for the obtaining of an aligned filler structure within a thermoplastic matrix. For this study, Poly(Ethylene-co Vinyl Acetate) (EVA), revealed as a biocompatible polymeric matrix, was combined with barium titanate (BaTiO₃) filler, well-known as a lead-free piezoelectric material. The phase inversion method was used to obtain an optimal dispersion of the BaTiO₃ within the EVA thermoplastic matrix. The effect of the processing parameters, such as the poling electric field and the filler content, were analyzed via dielectric spectroscopy, piezoelectric characterization, and scanning electron microscopy (SEM). The thermal behavior of the matrix was investigated by thermogravimetric analysis (TGA) and differential scanning calorimetry analysis (DSC). Thermoplastic-based structured composites have numerous appealing advantages, such as recyclability, enhanced piezoelectric activity, encapsulation properties, low manufacturing time, and being light weight, which make the developed composites of great novelty, paving the way for new applications in the medical field, such as integrated sensors adaptable to 3D printing technology. Full article

The performance and programming conditions of the triple shape memory of crosslinked trans-polyisoprene/poly (ethylene-co-vinyl acetate) (TPI/EVA) composites with different contents of dicumyl peroxide (DCP) were investigated. The effect of triple shape memory in the TPI/EVA composites was studied by tensile loading, scanning electron microscopy (SEM), differential scanning calorimetry (DSC), and dynamic thermomechanical analysis (DMA). It was demonstrated that the content of DCP increased, the crystallization temperature of TPI decreased from 55.2 to 38.3 °C, and the crystallization temperature of EVA decreased slightly. The SEM results showed that DCP, as an initiator, could form a graft copolymer of TPI-g-EVA at the interface of the two phases, which could improve the adhesion of the two phases. The DMA showed that the higher the content of DCP, the higher the first-stage shape recovery ratio. Moreover, the composites exhibited favorable shape fixity ratio (R_f) and shape recovery ratio (R_r) with the incorporation of 0.4 phr DCP. At the same time, it was demonstrated that the TPI/EVA composites showed excellent mechanical strength, including tensile strength up to 24.3 MPa, as well as elongation at break reaching 508%. Full article

Flexible antibacterial materials have gained utmost importance in protection from the distribution of bacteria and viruses due to the exceptional variety of applications. Herein, we demonstrate a readily scalable and rapid single-step approach for producing durable ZnO nanoparticle antibacterial coating on flexible polymer substrates at room temperature. Substrates used are polystyrene, poly(ethylene-co-vinyl acetate) copolymer, poly(methyl methacrylate), polypropylene, high density polyethylene and a commercial acrylate type adhesive tape. The deposition was achieved by a spin-coating process using a slurry of ZnO nanoparticles in toluene. A stable modification layer was obtained when toluene was a solvent for the polymer substrates, namely polystyrene and poly(ethylene-co-vinyl acetate). These coatings show high antibacterial efficiency causing >5 log decrease in the viable counts of Gram-negative bacteria Escherichia. coli and Gram-positive bacteria Staphylococcus aureus in 120 min. Even after tapping these coated surfaces 500 times, the antibacterial properties remained unchanged, showing that the coating obtained by the presented method is very robust. In contrast to the above findings, the coatings are unstable when toluene is not a solvent for the substrate. Full article

Poly (ethylene-co-vinyl acetate) (PEVAc) is a copolymer endowed with high elasticity and resilient properties, potentially utilized in various applications. However, the tensile strength of this copolymer is insufficient for use in certain applications that require enough strength to tolerate high external tension or stress. In this study, dolomite was proposed as a nanofiller to reinforce the PEVAc. Raw dolomite was physically and chemically modified in order to improve its mix ability and interfacial adhesion between the PEVAc and dolomite. Initially, the size of dolomite was reduced by combining the ball-milling and tip-sonication methods. SEM, TEM, and XRD were used to characterize the morphology/structure of the raw dolomite and the size-reduced dolomite. Then, a particle size analysis was performed to confirm the average particle size. Our results show that the particle size of dolomite was reduced from 150 µm to 441.4 nm by the physical modification process (size reduction). Based on the TEM analysis, the Feret diameter (d_f) of the dolomite particles was also reduced from ~112.78 µm to ~139.58 nm only. This physically modified dolomite is referred as dolomite nanoparticles (DNPs), since one or more of its dimensions is less than 100 nm (e.g., thickness and width). To further improve the dolomite and PEVAc matrix interactions, chemical modification of the DNPs were performed by treating the DNPs with stearic acid, forming non-polar dolomite nanoparticles (NP-DNPs). The presence of stearic acid in dolomite was confirmed through FTIR and contact angle analyses. A PEVAc nanocomposite film with NP-NPDs as a nanofiller appeared more homogeneous and exhibited the highest increment in tensile strength and elongation at break. These findings indicated that the combination of ball milling and tip sonication is an efficient method for producing very fine dolomite particles up to the nano-size range, whereas chemical surface modifications improved the compatibility between the dolomite and the copolymer. The combination of these physical and chemical modifications helped to develop a homogeneous copolymer nanocomposite system with improved tensile properties. Full article

Technological developments in the solar photovoltaic field must guarantee the high performance and low deterioration of solar cells in order for solar power plants to be more efficient and competitive. The solar cell needs comprehensive protection offered by a polymeric encapsulant, which improves UV stability, reduces water and moisture absorption, reduces oxygen and vapor permeability and enhances mechanical resistance. Moreover, high transparency and adhesion yields improved the solar panel performance. The current work analyzes polymeric films based on poly(ethylene-co-vinyl acetate) (EVA) and polyolefin (PO) for photovoltaic encapsulant use (the high temperature resistance is improved by adding PO to EVA, as investigated and documented before). To enhance the mechanical resistance and optical properties of the investigated matrices, a crosslinking agent, an adhesion promoter and stabilizing agents have been incorporated in both EVA and EVA/PO systems. The adhesion promoter is a polar wax–silane-free agent; the absence of the silane function allows the integrity of the module to be maintained over time. All samples were characterized through mechanical and rheological analysis, and their long-term UV stability was investigated by accelerated ageing and by FTIR and UV–vis spectroscopy. The obtained results suggest that the presence of a crosslinking agent, an adhesion promoter and stabilizers in EVA/PO-based films allows for the achievement of the required features for the encapsulants, showing mechanical and rheological behavior similar to those of EVA containing the same additives. Full article

It was found that the use of natural magnesium hydroxide (n–MDH) as mineral filler in EVA based composites provided mechanical and rheological properties that did not completely comply with the halogen-free flame-retardant (HFFR) cables parameters. Moreover, the use of n–MDH mostly gave a rough grey surface in the compound extruded by rheometry capillary. In contrast, with the use of synthetic material (s–MDH), a combination of better outcomes was observed. Mechanical and rheological properties were more aligned with the application, and the aesthetics were also improved, i.e., the surface was smooth and whiter. Therefore, with the aim of obtaining good aesthetical quality on the extrudate, we studied formulations by varying the type of polymer matrix and using a mixture of the natural magnesium hydroxide combined with other kind of fillers (in a 3:1 ratio using as main filler n–MDH). On this account, we found a synergistic effect in the mechanical, rheological, and aesthetic properties for the filler blend system containing n–MDH in combination with s–MDH or Böhmite AlO(OH), or using a secondary polymer belonging to the polybutene family combined with EVA. Full article

In recent pharmaceutical applications, an active pharmaceutical ingredient (API) can be mixed with a polymer material to yield a composite long-acting drug-delivery device. These devices boast higher patient compliance, localized drug delivery, and lower dosage concentrations, which can increase patient safety. As a laboratory-safe option, calcium carbonate (CaCO₃) was used as a drug surrogate to mimic the release kinetics of a low-solubility API. The release of CaCO₃ from a poly(ethylene vinyl acetate) (EVA) polymer matrix was studied in ultra-high-purity water. The geometry of CaCO_3, along with the manufacturing technique, was manipulated to study the implications on surrogate drug release. It was found that injection molding proved to yield higher burst release, due to higher pressures achievable during manufacturing. The extrusion process can affect the surface concentration of the pharmaceutical ingredient when extruded through a water bath, resulting in a lower initial burst concentration. Regarding CaCO₃ geometry, the particle size was more critical than the surface area in terms of CaCO₃ release. Larger particles showed a higher release rate, though they also displayed higher variability in release. These data can be used to engineer specific release profiles when designing composite formulations and manufacturing methods for pharmaceutical-drug-delivery applications. Full article

In this work, we study the effect of strong electric fields on a polymer/graphene composite and the resulting morphology upon its dielectric breakdown. Our model system was produced by compounding up to 0.25 wt % graphene nanoplatelets (GNP) into poly(ethylene-co-vinyl acetate) (EVA), which is a soft polymer with low melt viscosity. A strong electric field of up to 400 V_rms/mm was applied to the EVA/GNP composite in the melt. The sample’s resistance over the electric field application was simultaneously measured. Despite the low GNP loading, which was below the theoretical percolation threshold, the electric conductivity of the composite during electric field application dramatically increased to >10⁻⁶ S/cm over 5 min of electric field application before reaching the current limit of the experimental apparatus. Conductivity growth follows the same scaling relationship of the theoretical model that predicts the rotation and translation time of GNPs in a polymer melt as a function of electric field strength. Since no significant GNP alignment in the composite was observed under transmission electron microscopy (TEM), we hypothesized that the increase in electrical conductivity was due to local electrical treeing of the polymer matrix, which eventually leads to dielectric breakdown of the composite. Electrical treeing is likely initiated by local GNP agglomerates and propagated through conductive channels formed during progressive dielectric breakdown. Full article

A series of coatings from poly(ethylene-co-vinyl acetate) (EVA) were obtained using the matrix-assisted pulsed laser evaporation (MAPLE) technique. By changing the process parameters, i.e., laser fluence and EVA co-polymer concentration in the target, coatings with various morphologies and topographies were produced. The evaluation of the film structure was based on an analysis of optical and atomic force microscopy and profilometry measurements. A detailed chemical structure investigation, conducted based on Fourier transform infrared (FTIR) and X-ray photoelectron spectroscopy (XPS) spectra, revealed that although the general structure was preserved, some alterations of ethylene (Et) and vinyl acetate (VAc) blocks took place. The most noticeable change was in the ester group that was transformed into ketone and carboxyl groups; nevertheless, some changes in the aliphatic main chain were also present. The chemical structure changes in EVA coatings took place regardless of the process parameters used. The use of chloroform as a solvent to dissolve the EVA copolymer was indicated as a possible reason of the changes as well as the tendency of EVA macromolecules to form clusters. Nevertheless, due to low level of structure alteration, it has been shown that the MAPLE technique can be successfully used to obtain coatings from polymers with more complex structures, which are soluble in a limited number of solvents. Full article