Search Results (105)

In this work, we report the effect of combining styrene-vinyl tetrazole copolymer (StVTz) and ammonium polyphosphate (APP) on the thermal degradation, mechanical properties, flame retardancy, and char formation of low-density polyethylene with ethyl vinyl acetate (LDPE/EVA) composites. The tetrazole heterocycle exhibits high thermal stability (>200 °C), and during its thermal decomposition, it releases non-toxic nitrogen gas. Its degradation generates reactive species capable of cross-linking the polymer chains, thereby promoting the formation of a protective char layer. To evaluate the influence of composition on the intumescent flame-retardant (IFR) properties of LDPE/EVA blends, different concentrations of APP and StVTz additives were incorporated. The composites were prepared in an internal mixer (Brabender Intelli-Torque Plasti-Corder). Test specimens were obtained by compression molding and subsequently cut into appropriate shapes for each analysis. Thermal stability was studied by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). Mechanical properties were evaluated by tensile testing. Morphology of cone calorimetry (CC) residues was examined using SEM. Flammability properties, studied using CC, revealed a 70% reduction in the peak heat release rate (pHRR) and a 48% reduction in the total heat release (THR) compared to the neat LDPE/EVA blend. These results indicate that StVTz and APP act synergistically to improve the flame-retardant properties of LDPE/EVA. Full article

Ethylene–vinyl acetate (EVA) is a versatile polymer for applications in dental devices; however, its vulnerability to microbial colonization increases with long-term use. This study evaluates EVA composites modified with silver–sodium–hydrogen–zirconium phosphate (SP) particles, aimed at enhancing antimicrobial performance while preserving key functional properties. Composites containing 1–16 wt.% SP were prepared via solvent-based and mechanical compounding routes, with scanning electron microscopy confirming correct filler distribution across processing methods. Antimicrobial assays revealed a pronounced reduction in Streptococcus mutans and Candida albicans levels, reaching 88% and 98% antimicrobial efficacy, respectively, at 16 wt.% SP. Cytotoxicity testing with L-929 fibroblasts demonstrated maintained cell viability above the 70% threshold, confirming non-cytotoxicity. Mechanical characterization indicated marginal increases in hardness, slight tensile strength reduction at higher filler loadings, while other physicochemical and thermal analyses showed minimal impact on polymer performance. These findings indicate balanced antimicrobial activity with other biofunctional properties. Full article

As an eco-friendly flame-retardant additive, magnesium hydroxide (MH) is widely employed in low-smoking, halogen-free polymer materials due to its environmentally benign nature. In order to enhance flame retardancy performance, the modified MH was modified with tetrakis(hydroxymethyl)phosphonium sulfate (THPS) by a one-pot hydrothermal method. The resulting morphology was characterized using scanning electron microscopy (SEM), and it shows the dispersion of nanometer particles and almost no aggregation. The X-ray photoelectron spectroscopy (XPS) along with Raman spectroscopy show that the THPS is connected with the Mg(OH)₂ by chemical bond. The sample was incorporated into ethylene–vinyl acetate (EVA) to evaluate the flame retardancy was assessed via limiting oxygen index (LOI) and vertical burning tests (UL-94). The results show that THPS modified MH effectively enhanced the flame retardancy, achieving a V-0 rating and an LOI value of 31.3%. In addition, the composites retain good mechanical integrity. The thermal analysis with TGA and DTG shows the formation of the MgO decomposition product, along with water vapor and phosphorus-containing radicals released by modified MH in the combustion process, forming a strong flame-retardant protective layer. In addition, the maximum smoke density of EVA/MHP-3 composite was 155.4, lower than 411.3 for EVA/MH, with a 62.2% reduction in total smoke production. The result shows that THPS is effective for improving the flame-retardant efficiency of inorganic metal hydroxide in polymer composites. Full article

The article presents the results of a study of the possibility of using heat-treated ethylene-vinyl acetate copolymer (EVA) as a thermoplastic modifier in a photosensitive composition based on tert-butyl acrylate (tBA). The use of such a modifier in 3D printing compositions is important for improving their physical and mechanical properties at low temperatures. An attempt was also made to use EVA as a polymer chain brancher. The molecular structure of the components and their compositions, rheology, curing kinetics, and phase organization of photocured systems were studied using FTIR and NMR spectroscopy, spectrophotometry, rheometry, Photo-DSC, and scanning electron microscopy. It was found that heat treatment of EVA allows the formation of single C=C bonds in macromolecules, which are necessary for a potential crosslinking agent with tBA. It was shown that EVA effectively functions as a thickener and modifier: with an increase in the modifier concentration, the nature of the composition flow changes from Newtonian to pseudoplastic, the rate of the photochemical polymerization reaction decreases, and the degree of conversion of the system decreases. However, the formation of a heterogeneous phase structure and the absence of a continuous spatial network of chemical bonds prevent the use of EVA simultaneously as a functional additive and crosslinking agent. Full article

Preventing soil degradation caused by water erosion is essential for sustainable agriculture and long-term agroecological development. The objective of this study was to evaluate the effectiveness of an ethylene-vinyl acetate (EVA) polymer-based soil conditioner in mitigating soil erosion, a key driver of soil degradation. Laboratory experiments and simulations employing the Water Erosion Prediction Project (WEPP) model were conducted to assess soil erodibility parameters and sediment yield of two soil types from Okinawa, Japan. A key contribution of this work is the integration of these experimentally determined erodibility parameters into the WEPP model for robust validation. Interrill and rill erosion processes were analyzed under different soil conditioner application rates. Laboratory results showed that applying the soil conditioner reduced interrill erodibility by 59 to 99% and rill erodibility by 65 to 100%, while increasing critical shear stress and water infiltration rate. The effectiveness varied between the two soil types due to differences in particle-size distribution and inherent erodibility. The soil conditioner exhibited a more pronounced impact on rill erosion. WEPP simulations confirmed sediment yield reductions of 73% to 99%, primarily influenced by changes in rill erodibility and critical shear stress. While its practical application will be subject to various field conditions, our findings confirm the significant potential of this soil conditioner as a strategy for preserving topsoil resources. Full article

This work reports the fabrication of innovative flexible conductive polymer composites (FCPCs), composed of poly (2,3-dihydrothieno-1,4-dioxin)-poly (styrenesulfonate) (PEDOT:PSS), polypyrrole (PPy) and copper phthalocyanine (CuPc). These FCPCs were deposited by the drop-casting technique on flexible substrates such as polyethylene terephthalate (PET), Xuan paper and ethylene–vinyl acetate (EVA) foam sheets. Wearable photoactive electrocardiogram (ECG) electrodes and flexible strain sensors were fabricated. Morphological characterization by SEM revealed a stark contrast between the smooth, continuous PEDOT:PSS films and the rough, globular PPy films. EDS confirmed the successful and homogeneous incorporation of the CuPc, evidenced by the strong spatial correlation of the nitrogen and copper signals. The highest mechanical resistance was present in the FCPCs on PET with a limit of proportionality between 4074–6240 KPa. Optical parameters were obtained by Ultraviolet–Visible Spectroscopy and their Reflectance is below 15% and could be used as photoelectrodes. Three Signal Quality Indexes (SQIs) were used to evaluate the ECG signal obtained with the electrodes. The results of all the SQIs demonstrated that the obtained signals have a comparable quality to that of a signal obtained from commercial electrodes. To evaluate the flexible strain sensors, the change in output voltage caused by mechanical deformation was measured. Full article

The aim of this study was the hydrothermal leaching of silver from waste monocrystalline silicon (m-Si) and polycrystalline silicon (p-Si) photovoltaic panel (PV) cells using organic acids, namely oxalic acid (OA) and citric acid (CA). Before leaching, two different pretreatment procedures were applied. First, the fluoropolymer backsheet was manually removed from the panel pieces and, then, the samples were subjected to high-temperature heating for the thermal degradation of the ethylene vinyl acetate (EVA) polymer. When removal by hand was not feasible, the second pretreatment procedure was followed by toluene immersion to remove the EVA and backsheet and separate the cells, glass, and films. After pretreatment, 4 M HCl leaching was applied to remove the aluminum layer from the cells. The remaining cells were subjected to hydrothermal leaching with organic acids to extract the silver. Several hydrothermal parameters were investigated, such as acid concentration (1-1.5-2 M), processing time (60-105-150 min), and temperature (150-180-210 °C), while the liquid-to-solid (L/S) ratio was fixed at 30 mL: 1 g, based on preliminary tests. Response surface methodology (RSM) was applied to optimize the hydrothermal leaching parameters. The optimized parameters were 210 °C, 95 min, 2 M CA or 210 °C, 60 min, 1 M OA. OA was more effective in Ag leaching than CA. The results were compared to HNO₃ leaching. The green leaching of silver from end-of-life PV panels with organic acids is an environmentally beneficial route. Full article

The high-temperature performance of well cement is critical for the construction of deep geothermal wells and high-temperature energy storage wells, where mechanical integrity and pore structure stability govern wellbore reliability. To address the strength degradation and structural deterioration of conventional cements under high temperature, the G-class cement was modified by ethylene-vinyl acetate (EVA) polymer and polypropylene fibers (PF), and their impact under various temperatures was explored. Results show that at 600 °C, the compressive strength of modified cement remains above 30 MPa. While the cumulative pore area decreases at 500 °C, a significant increase in larger pores and a major restructuring of the pore network occurs at 600 °C, reflecting the dual effects of high temperature on the pore structure. The modified cement retains structural integrity and excellent mechanical performance up to 400 °C with minimal strength loss, uniform strain distribution, and stable pore structure. At 500 °C and above, it still maintains load-bearing capacity and deformation adaptability, meeting the service requirements for geothermal wells and high-temperature energy storage wells. Even at 600 °C, the reinforcing effect of EVA and PF degradation products slow down crack propagation, ensuring durability in extreme conditions. The research findings lay the foundation for the development of well cement for high-temperature service environments. Full article

The application of graphene nanoplatelets (GNPs) in polymer composites is a challenge due to their high tendency to agglomerate and restack during processing. In this work, alkyl phosphonium-based ionic liquid was used to assist the dispersion of GNP in an ethylene-vinyl acetate (EVA) matrix, through a melt-mixing procedure. The mechanical properties and creep resistance of the films prepared by the film extrusion process were evaluated. The results demonstrated that the noncovalent treatment of GNP with the ionic liquid (IL) enhanced the electrical conductivity and creep stability of the EVA composites. The microwave absorbing properties were studied in the X-band and Ku-band. A reflection loss (RL) of −15 dB for EVA containing 0.5 wt% of GNP and 1:1 wt% of GNP/IL was achieved. The use of a multi-layered structure containing thin film layers was efficient for enhancing the microwave absorbing performance, with a minimum RL of −24.6 dB and effective absorption bandwidth of 4.3 GHz. This result is attributed to the internal reflection and scattering of the radiation between layers. The use of simple, low-cost materials and procedures, combined with the system’s excellent mechanical and electrical properties, makes it a promising candidate for multifunctional applications as electrostatic dissipative and microwave absorbing materials for electronic packaging and other electronic devices. Full article

Poly(L-lactic acid) (PLLA) was blended with an ethylene-vinyl acetate (EVA) copolymer, which is generally recognized as a phase-separated system. The interactions between these polymer species were examined via spherulite observation. The PLLA/EVA blend was concluded to be a partially miscible system. The onset temperature for the crystallization of PLLA, as the crystalline polymer, systematically changed when PLLA was blended with EVA at various ratios. The glass transition behavior of EVA was almost absent in the thermogram when the PLLA:EVA blend ratio was greater than 2:1. The spherulite size distribution of PLLA became finer as the PLLA:EVA ratio was changed from 3:1 to 2:1 to 1:1, and observing spherulites was difficult when the blend ratio was 1:2. Because the nucleation position was different each time during the repeated melting/crystallization of spherulites, this system exhibited homogeneous nucleation. In addition, in a plot of the spherulite size versus the crystallization time, the inclination angle changed between the PLLA/EVA = 3:1 and 2:1 blends, and the critical ratio at which the crystallization behavior changed was estimated. Full article

Recently, there has been a rapid growth in the use of biodegradable polymers as alternatives to petroleum-based polymers, particularly in the packaging sector, to reduce environmental pollution. In this scenario, the aim of this work was to study the use of different amounts of Natamycin on two polymer systems: one that is non-biodegradable but widely known in the field of packaging and one that is biodegradable and is emerging as a possible replacement, in order to accelerate progress toward the achievement of the sustainable development goals. Both systems were produced through melt mixing followed by compression moulding. Subsequently, they were fully characterized by rheological, morphological, mechanical, thermal, and wettability analyses. Natamycin release was evaluated in water at 4 °C by UV-Vis measurements. The antifungal activity of both polymeric systems containing Natamycin was assessed in vitro against three strains of undesirable filamentous fungi of food interest. The results show that PCL with 5% Natamycin represents an effective biodegradable alternative to EVA for inhibiting undesirable filamentous fungi. More specifically, both systems at 5% showed comparable inhibition zones of about 30 mm. Full article

Aluminum hydroxide (ATH) is an environmentally friendly flame retardant widely employed in polymers. However, the high loading of ATH, due to its limited efficiency, potentially compromises other properties, including mechanical properties. This work explores a feasible ball milling strategy for high-efficiency ATH-based flame retardants (PPA-ATH and PPOA-ATH), fabricated by employing phenylphosphinic acid (PPA) and phenylphosphonic acid (PPOA) as surface modifiers and water as the processing solvent. The characterization study of PPA-ATH and PPOA-ATH demonstrates that ball milling effectively reduces their particle size, enhances their specific surface area, and improves their dispersibility within the ethylene-vinyl acetate (EVA) matrix. PPOA-ATH exhibited superior capabilities in enhancing the thermal stability and flame retardancy of EVA composites compared to PPA-ATH. The incorporation of PPOA-ATH resulted in the retarding in the temperature at 50% mass loss by 21 °C and an increase in the char residue of 34.5% at 700 °C. Furthermore, PPOA incorporation led to reductions of 81.0% in the peak heat release rate, 48.1% in the total heat release, 73.7% in the peak smoke production rate, and 41.2% in the total smoke production compared to neat EVA. This green modification strategy successfully addresses the application limitations of ATH, providing a feasible and environmentally friendly method for high-efficiency ATH-based flame retardant fabrication. Full article

To investigate the influence of factors such as tourism, agriculture, and population density on the presence of microplastic (MP) content in aquatic environments and their associated ecological risks, Jingpo Lake, a remote high-mountain lake situated away from urban areas, was selected as the research subject. This study examined the abundance, types, sizes, colors, and polymer compositions of MPs within the water body, fish, and sediments. By considering variables, including fishing practices, agricultural activities, population dynamics, and vegetation cover, an analysis was conducted to unravel the spatial and temporal distribution of MPs concerning human activities, ultimately leading to an assessment of the ecological risks posed by MP pollution. The findings revealed that the average abundance of MPs in the lake’s surface water was recorded as (304.8 ± 170.5) n/m³, while in the sediments, it averaged (162.0 ± 57.45) n/kg. Inside the digestive tracts of fish, the MP abundance was measured at 11.4 ± 5.4 n/ind. The contamination of MPs within the aquatic environment of Jingpo Lake was found to be relatively minimal. Variations in MP loads across time and space were observed, with MPs predominantly falling within the size range of small planktonic organisms (50–1000 μm). Additionally, the prevalent colors of MPs in the water samples were white or transparent, constituting approximately 55.65% of the entire MP composition. Subsequently, they were black, red, and blue. This colors distribution were consistent across MPs extracted from fish and sediment samples. The chemical compositions of the MPs predominantly comprised PE (31.83%) and PS (25.48%), followed by PP (17.56%), PA (11.84%), PET (6.71%), EVA (4.56%), and PC (2.03%). Regarding the seasonal aspect, MP concentrations were highest during summer (46.68%), followed by spring (36.75%) and autumn (16.56%). The spatial distribution of MPs within Jingpo Lake’s water body, fish, and sediments was notably influenced by human activities, as confirmed by Pearson correlation coefficients. A strong association was observed between MP levels and water quality indicators such as ammonium nitrogen (NH₄-N), total phosphorus (TP), and chlorophyll-a (Chla), suggesting that human-related pollution contributed significantly to MP contamination. The diversity assessment of MP pollutants exhibited the highest variability in chemical composition (1.23 to 1.79) using the Shannon–Wiener Index. Subsequently, the diversity of colors ranged from 0.59 to 1.54, shape diversity from 0.78 to 1.30, seasonal diversity from 0.83 to 1.10, and size diversity from 0.44 to 1.01. The assessment results of ecological risk highlighted that the risk categories for MPs within the surface water, fish, and sediments of Jingpo Lake were categorized as I for the PHI and PLI and as “Minor” for the PERI. These relatively low-risk values were attributed to the predominantly low toxicity of the distributed MPs within the Jingpo Lake basin. Moreover, the results of the risk assessment were found to be interconnected with the distribution of the local population and agricultural activities around the sampling sections. Usage patterns of coastal land and population density were recognized as influential factors affecting MP loads within the water body, sediments, fish, and other components of the lake ecosystem. Full article

In the present work, carbonate minerals are added in non-polar and polar polymer matrices to develop halogen-free flame-retardant composites. The examined fillers of calcium carbonate and magnesium carbonate delivered improved rheological performance in both non-polar (PE) and polar (EVA/PE) polymer compounds compared to the natural magnesium hydroxide and huntite/hydromagnesite mineral fillers. The presence of EVA in the matrix enhanced the mechanical behavior of all compounds in tensile testing. The thermal stability of the composites was particularly improved for the polar systems with the incorporation of the carbonate minerals, as this was evidenced under thermogravimetric analysis. The dielectric behavior of the fabricated systems was examined via broadband dielectric spectroscopy. The HFFR compounds attained higher values of the real part of dielectric permittivity from the unreinforced systems in the whole frequency and temperature range of the conducted tests. This behavior is ascribed to the higher permittivity values of the fillers with respect to the polymer matrices and the occurrence of interfacial polarization. All minerals improved the flame retardancy of the compounds in terms of LOI values, while the addition of EVA yielded further improvements, especially for the magnesium carbonate and the magnesium hydroxide minerals. Full article

This work studied biocomposites based on a blend of low-density polyethylene (LDPE) and the ethylene–vinyl acetate copolymer (EVA), filled with 30 wt.% of cellulosic components (microcrystalline cellulose or wood flour). The LDPE/EVA ratio varied from 0 to 100%. It was shown that the addition of EVA to LDPE increased the elasticity of biocomposites. The elongation at break for filled biocomposites increased from 9% to 317% for microcrystalline cellulose and from 9% to 120% for wood flour (with an increase in the EVA content in the matrix from 0 to 50%). The biodegradability of biocomposites was assessed both in laboratory conditions and in open landfill conditions. The EVA content in the matrix also affects the rate of the biodegradation of biocomposites, with an increase in the proportion of the copolymer in the polymer matrix corresponding to increased rates of biodegradation. Biodegradation was confirmed gravimetrically by weight loss, an X-ray diffraction analysis, and the change in color of the samples after exposition in soil media. The prepared biocomposites have a high potential for implementation due to the optimal combination of consumer properties. Full article