Search Results (116)

Fabric veneer panels were prepared using ethylene-vinyl acetate copolymer film (EVA) as the intermediate layer and poplar plywood as the substrate. Eight fabrics with different compositions were selected for evaluation to screen out fabric materials suitable for poplar plywood veneer. The fabrics were objectively analyzed by bending and draping, compression, and surface roughness, and subjectively evaluated by establishing seven levels of semantic differences. ESEM, surface adhesive properties, and peel resistance tests were used to characterize the microstructure and physical–mechanical properties of the composites. The results show that cotton and linen fabrics and corduroy fabrics are superior to other fabrics in performance, and they are suitable for decorative materials. Because the fibers of the doupioni silk fabric are too thin, and the fibers of felt fabric are randomly staggered, they are not suitable for the surface decoration materials of man-made panels. The acetate veneer surface gluing performance was 1.31 MPa, and the longitudinal peel resistance was 20.98 N, significantly exceeding that of other fabric veneers. Through the subjective and objective analysis of fabrics and gluing performance tests, it was concluded that, compared with fabrics made of natural fibers, man-made fiber fabrics are more suitable for use as surface finishing materials for wood-based panels. The results of this study provide a theoretical basis and process reference for the development of environmentally friendly decorative panels, which can be expanded and applied to furniture, interior decoration, and other fields. 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

This study investigated the effects of electron beam radiation on the room-temperature and high-temperature mechanical properties of two ethylene-vinyl acetate (EVA) copolymers, designated EVA 206 and EVA 212. These copolymers had varying vinyl acetate (VA) contents (6 wt.% and 12 wt.%), with the same melt flow index of 2.0 g/10 min. Samples were irradiated at doses ranging from 60 to 180 kGy. The impact of electron beam irradiation on the creep, frequency sweep, and stress–strain behaviors of the ethylene-vinyl acetate copolymers was evaluated using a dynamical mechanical analyzer (DMA). Crystallinity was measured using differential scanning calorimetry (DSC) and wide-angle X-ray diffraction (WAXD). Creep compliance was quantitatively analyzed using four-parameter and six-parameter models. While crosslinking had minimal influence on the room-temperature properties, it significantly affected the behavior at 150 °C. With increasing irradiation dose, creep compliance decreased, while the shear modulus, viscosity, and shear stress at a strain of 0.03 increased, indicating enhanced resistance to deformation. Crosslink density also increased with irradiation dose. EVA 212 with a higher vinyl acetate content exhibited a higher resistance to creep and better high-temperature mechanical properties across all measurements. Full article

The properties of EVA copolymers with various vinyl acetate (VA) contents were compared, with EVA 206 (6 wt.% VA) and EVA 212 (12 wt.% VA) having the same melt flow indices of 2 g/10 min. The impact of electron irradiation at levels of 60, 120, and 180 kGy was studied. Four testing methods were employed as follows: wide-angle X-ray diffraction (WAXD); differential scanning calorimetry (DSC); dynamic mechanical analysis (DMA), using a high-temperature frequency sweep at 150 °C; and gel content analysis. The amount of crystalline phase was determined by WAXD and DSC. Copolymers with a higher VA content (EVA 212) had lower crystallinity. The increase in the amorphous phase allows for the greater movement of radicals, enabling them to react and form cross-links. The effects of the VA content, radiation dose, and frequency on dynamic mechanical properties were investigated by DMA. The DMA analysis focused on the shear storage modulus $G^{\prime }$, damping factor $\tan \delta$, and complex viscosity ${\eta }^{*}$. After irradiation, the damping factor $\tan \delta$ decreased with an increasing VA content, indicating improved elasticity and a higher degree of cross-linking. A gel content analysis was used to calculate the parameters of the Charlesby-Pinner and Charlesby–Rosiak equations, which help with the determination of the relationship between cross-linking and chain scission. The ratio of cross-linking to scission $G\left(X\right)/G\left(S\right)$ was higher for the EVA with a higher VA content (EVA 212). Due to a higher VA content (12 wt.%), EVA 212 exhibits more efficient network formation. 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

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

Using solid waste-based materials, such as recycled building aggregate (RCA), preparing 3D-printed materials can reduce costs but increase the water–cement ratio of the printed material, which reduces its mechanical performance. In order to solve the problem of mechanical properties decline caused by an increase in the w/c ratio, this experiment found that adding calcined salt mud (CSM) to the printing materials and changing the water-to-cement ratio from 0.37 to 0.4 CSM can ensure that the compressive strength of the printing materials remains basically unchanged. Moreover, through TG, SEM, and other microscopic data, it can be seen that calcium hydroxide in CSM can not only participate in the synergistic reaction of ethylene/vinyl acetate copolymer (EVA) and dust ash (DA), produce more NaOH, and promote the hydration of granulated blast furnace slag (GBFS) but also promote the formation of ettringite together with SO₄²⁻ in solution, optimizing pore size distribution. Full article

We studied the rheological properties under both shear and elongational flow and crystallization behaviors after shear history for binary blends of poly(lactic acid) (PLA) and ethylene–vinyl acetate copolymer (EVA) with a slightly lower shear viscosity. EVA was immiscible with PLA and dispersed in droplets in the blend. The addition of EVA significantly reduced the shear viscosity, which is attributed to the interfacial slippage between PLA and EVA. In contrast, under elongational flow, the addition of EVA provided strain hardening in the transient elongational viscosity. Consequently, the degree of neck-in behavior in T-die extrusion, i.e., a decrease in the film width, was reduced with the high orientation of the PLA chains. Furthermore, it was found that the addition of EVA accelerated the shear-induced crystallization of PLA, although EVA showed no nucleating ability without a flow field. Because the EVA addition can improve the mechanical toughness, this modification technique is attractive for various industrial applications of PLA. 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

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

In this study, vinyl triethoxysilane (VTES), KH-560 and trimethylchlorosilane (TMCS) were used to modify the surface groups of commercially available nano-silica (SiO₂, 50 nm), and ethylene vinyl acetate copolymer (EVA) was used as a film-forming agent. EVA/SiO₂, EVA/V-SiO₂, EVA/K-SiO₂ and EVA/T-SiO₂ coatings were prepared, respectively. The coatings were characterized by SEM, FTIR, TG and contact angle. It was found that when the mass percentage of SiO₂ was 66 wt%, the hydrophobicity performance of the coating could be significantly improved by silica modification. Compared to the EVA/SiO₂, the water contact angle (WCA) of the EVA/V-SiO₂, EVA/K-SiO₂ and EVA/T-SiO₂ were increased by 24.0%, 14.4% and 24.6%, respectively. The FTIR results indicated that VTES, KH-560 and TMCS could effectively replace the -OH groups on the surface of the SiO₂ after hydrolysis, resulting in the presence of water transport groups on the SiO₂ surface. The TG results certified that TMCS had the highest substitution rate (24.6%) for the -OH groups on the SiO₂ surface after the hydrolysis. Additionally, the SEM results indicated that T-SiO₂ was more easily dispersed in the EVA film-forming agent, leading to a uniform micro–nano surface rough structure, which aligned with the Cassie–Wenzel model. The durability test had demonstrated that the EVA/T-SiO₂ maintained its hydrophobic properties even after enduring 40,000 drops of water and the impact of 200 g of sand. Furthermore, it exhibited excellent resistance to acid corrosion, along with superior self-cleaning properties and an anti-fog performance. It also provided outstanding protection against high temperatures and UV radiation for outdoor applications. Full article

Polyoxymethylene (POM), polypropylene (PP), and poly(methyl methacrylate) (PMMA) have been blended with adhesive-grade ethylene vinyl acetate (EVA), propylene elastomer (VMX), isobutylene–isoprene rubber (IIR) and an acrylic block copolymer (MMA-nBA-MMA). The blends were prepared using a two-roll mill and injection molding. The mechanical properties of the blends, such as tensile strength, tensile modulus, elongation at maximum load, and impact resistance, were investigated. The water contact angle, melt flow rate (MFR), and differential scanning calorimetry were ascertained to evaluate the blends. The blend samples exhibited the following properties: all POM/EVA blends showed reduced crystallinity compared to neat POM; the 80% PMMA/20% MMA-nBA-MMA blend showed improved impact resistance by 243% compared to the neat PMMA. An antiplasticization effect was observed for POM/EVA 1% blends and PMMA/EVA 1% blends, with MFR reduced by 1% and 3%, respectively. The MFR of the PP/IIR 1% blend increased by 5%, then decreased below the MFR near the polymer for the remaining IIR concentrations. Full article

Ethylene–vinyl acetate copolymer (EVA), a crucial elastomeric resin, finds extensive application in the footwear industry. Conventional chemical foaming agents, including azodicarbonamide and 4,4′-oxybis(benzenesulfonyl hydrazide), have been identified as environmentally problematic. Hence, this study explores the potential of physical foaming of EVA using supercritical nitrogen as a sustainable alternative, garnering considerable interest in both academia and industry. The EVA formulations and processing parameters were optimized and EVA foams with densities between 0.15 and 0.25 g/cm³ were produced. Key findings demonstrate that physical foaming not only reduces environmental impact but also enhances product quality by a uniform cell structure with small cell size (50–100 μm), a wide foaming temperature window (120–180 °C), and lower energy consumption. The research further elucidates the mechanisms of cell nucleation and growth within the crosslinked EVA network, highlighting the critical role of blowing agent dispersion and localized crosslinking around nucleated cells in defining the foam’s cellular morphology. These findings offer valuable insights for producing EVA foams with a more controllable cellular structure, utilizing physical foaming techniques. Full article

The effect of plant-based fillers on thermal resistance in highly filled biocomposites based on ethylene–vinyl acetate copolymer (EVA) was studied. Wood flour and microcrystalline cellulose were used as fillers. It was shown that the introduction of microcrystalline cellulose into EVA did not affect the thermal stability of the polymer matrix. In contrast, the introduction of wood flour into EVA led to a significant increase in the thermal stability of the entire biocomposite. Oxidation induction time increased from 0 (pure EVA) to 73 min (EVA + wood flour biocomposites). The low-molecular weight phenolic compounds contained in wood flour are likely able to diffuse into the polymer matrix, exerting a stabilizing effect. The discovered stabilizing effect is a positive development for expanding the possibilities of technological processing of biocomposites, including multiple processing. Full article

To explore and deal with the difficulty in curing cement-stabilized bases in desert environments, curing agents were prepared to enhance the curing effect on the base in this research. The composite curing agent was prepared through orthogonal experiments and the durability of the curing agent coating were studied by simulating a desert environment. Subsequently, the curing effect on the performance of bases was analyzed. Finally, the hydration degree of cement was studied via scanning electron microscope (SEM), thermogravimetric analysis (TG), and X-ray diffraction analysis (XRD), and the curing mechanism of the curing agent was explored. The results show that the composite (paraffin emulsion is the main component of the film, vinyl acetate-ethylene copolymer dosage is 20%, ethanol ester-12 dosage is 10%, and sodium silicate dosage is 18%) could effectively improve the water-retention performance (water-loss ratio: 2.36%) and mechanical properties of the specimen (7 d compressive strength: 7.48 MPa; 7 d indirect tensile strength: 0.70 MPa). The dry shrinkage coefficient of the specimen with composite curing agent was reduced by 116.26% at 28 days. The compressive strength of dry and wet freeze could reach 7.48 MPa and 6.88 MPa, respectively. The durability of the curing agent-coated base met the requirements of pavement performance in desert areas. The results of XRD, TG, and SEM indicated that the curing agent promoted hydration. In addition, the number of C-S-H gel and AFt crystals significantly increased. The curing difficulty of road bases in desert areas could be reduced effectively through the application presented in this study, which contributes to the conservation of natural and human resources. Full article