Ethylene Vinyl Acetate Blends Research Articles

Nitrogen ion beam radiation induced modification on physico-chemical properties of poly (vinyl chloride)/ethylene vinyl acetate blends

Nitrogen ion beam radiation induced modification on physico-chemical properties of poly (vinyl chloride)/ethylene vinyl acetate blends

Synergistic compatibilization effect on phase morphology evolution and properties of poly(ether-block-amide)/ethylene-vinyl acetate blends

We investigate the synergistic effect of ethylene-vinyl acetate grafted maleic anhydride (EVA-g-MAH) and styrene-ethylene-butene-styrene grafted maleic anhydride (SEBS-g-MAH) compatibilizers on the phase morphology evolution, thermal and mechanical properties of polyether-block-amide/ethylene-vinyl acetate (PEBA/EVA) blends. Phase morphology of PEBA/EVA blends shows that the size of dispersed phase decreases in the presence of either EVA-g-MAH or SEBS-g-MAH compatibilizer. The simultaneous use of these two compatibilizers further reduces the dispersed phase size, indicating the synergistic effect of compatibilization. Thermal behavior analysis of PEBA/EVA blends reveals that the crystallization temperature (Tc), the enthalpy of fusion (ΔHm) and the crystallinity of PEBA decrease, the melting point (Tm) remains relatively unchanged with increasing EVA content. Tc and ΔHm increase for PEBA/EVA blends in the presence of compatibilizer. The tensile strength and elongation at break of PEBA/EVA blends decrease first and then increase with increasing EVA content. The simultaneous addition of EVA-g-MAH and SEBS-g-MAH compatibilizers is efficient to significantly improve the mechanical properties of PEBA/EVA blends. For instance, the tensile strength increases from 5.7 to 11.4 MPa, and the elongation at break increases from 73.5% to 600.9% for PEBA/EVA (50/50) blend in the presence of dual compatibilizers compared to the uncompatibilized blend. Dynamic mechanical analysis and rheological behaviors demonstrate that the modulus and complex viscosity are higher in PEBA/EVA blends by the simultaneous addition of two compatibilizers compared with the blends in the presence of one compatibilizer, suggesting the enhancement of interfacial interactions between PEBA and EVA, and further confirming the synergistic effect of compatibilization.

The effect of expanded graphite and paraffin wax on the morphological, thermal, and rheological properties of PP/EVA blend

The study investigated the effect of paraffin wax, expanded graphite, and their dispersion on the properties of the blend of polypropylene (PP) and ethylene vinyl acetate (EVA). The idea is to reduce interfacial tension in blends of PP and EVA while enhancing the properties of blends in the process. The chosen optimum contents of the paraffin wax and EG in the 80/20 PP/EVA blend were 10 and 6 wt.%, respectively. The morphological features show that the expanded graphite (EG) particles had high affinity for each other. Moreover, EG filler particles are localized inside the minor EVA phase and some at the interface. Rheological properties revealed that the flow of the binary composites increased when 10 wt.% wax is added suggesting that wax enhanced the processability of the composites. The Cole-Cole plots deviated from the semi-circular arc suggesting heterogeneity in the blend and PP/EVA/Wax/EG composite. The addition of paraffin wax and EVA delayed crystallization of PP, while earlier crystallization of PP was promoted by the presence of EG. Generally, all samples caught fire after 10 s, started dripping and are thus given a V-2 rating according to the Underwriters Laboratories test standard 94 results (UL-94).

Effect of Ethylene-Vinyl Acetate on the properties of Polybutylene Terephthalate/ Ethylene-Vinyl Acetate polymer blends

This research study analyzes the influence of Ethylene-Vinyl Acetate (EVA) resin on the properties of Polybutylene Terephthalate (PBT)/EVA blends produced by injection molding technique. It is based on the fact that a way to recycle PBT from toothbrush bristles is needed. Mechanical samples were made by mixing EVA into PBT with 0, 5, 10, 15, 20, and 25% contents. The samples were tested for flexural strength, impact strength, and hardness according to the standards of ASTM D790, ASTM D256, and ASTM D2240, respectively. The results show that when increasing the EVA content in the PBT/EVA blends, the flexural strength tends to decrease; the hardness fluctuates along a decreasing trend; however, the decrease is not significant. Interestingly, the measured impact resistance results are very positive, especially at the highest increase point, increasing by 40.7% compared to neat PBT. The microstructure results showed a good dispersion of EVA on the PBT substrate, but there was no compatibility between these two polymers. The results of XRD analysis showed that when EVA was mixed, it increased the crystallinity and improved the crystal growth of the blends.

Thermal, mechanical, rheological and morphological properties of compatible poly(lactic acid)/ethylene vinyl acetate blends

This paper examines the effects of poly (ethylene-co-vinyl acetate) (EVA) with 40% vinyl acetate content on thermal, mechanical, rheological, and morphological properties of polylactic acid (PLA) blends. Thermal analysis indicated improvement of crystallinity in the presence of more EVA. With 15% EVA, the impact strength of the binary blend increased significantly (37.80 KJ/m2) at an optimum elongation at break due to the compatibility of the blend and the formation of fibrils. In the presence of % EVA, complete phase separation with the formation of EVA droplets in the PLA continuous phase resulted in a reduction of impact strength and elongation at break. Changes in compatibility and morphology lead to variation in rheological properties. The complex viscosity (η*) decreased with increasing EVA content up to 10% EVA but slightly increased at 15% EVA due to optimum interphase interaction between components in the compatible blend. In the presence of more than 20% EVA, η* reduced again due to the occurrence of phase separation. The variations in the mechanical and rheological properties of PLA/EVA blends are directly related to the state of compatibility and morphology of the blends.

Recycling EVA Waste: An Opportunity for the Footwear Industry-Rheological Properties of EVA Waste Composites Using Torque Rheometry

Ethylene vinyl acetate blends (EVA-B) (at 19 and 28 wt% vinyl acetate) were supplied by the footwear industry, along with an industrial (reference) compound labeled EVA-ref. EVA waste is an industrial sub-product crosslinked (injection sprues and unused midsoles), that was particulate through a micronization process and labeled as EVA-w. The objective of the present work was to evaluate processability and rheological parameters (using torque rheometry) when adding EVA-w to EVA-B. The EVA-w particle size distribution was bimodal, with an average diameter of 53.06 μm, and volume (%) D (10), D (50), and D (90) respectively equal to 12.47, 31.83, and 135.18 μm. However, this ample size distribution did not affect the composite mixing. FTIR-ATR analysis showed that no new crosslinking occurred after processing the composites. Low unit mixing energy (Wu), and mechanical work (as represented by ΔT values: torque stabilization temperature (Tstab)−test temperature (Ttest)) were required to mix the composites. Consequently, the dispersion of the EVA-w particles within the molten EVA-B occurred during the first 3 min of mixing, making it easier. The sensibility to shear-thinning behavior was more pronounced when adding EVA-w, especially at 25 phr. The m parameter was smaller in the composites as compared to the EVA-ref, and when adding EVA-w at 35 phr, it showed a tendency to increase. The average shear stress (\(\overline{\tau }\)) of the 15 phr composite was similar to that of the EVA-ref compound. Yet for 25 phr, a higher value was observed. The adding of EVA-w made the non-Newtonian behavior of EVA-B less pronounced. For all samples, the average viscosity (\(\overline{\upeta }\)) decreased with average shear rate (\(\overline{\dot{\gamma } }\)), revealing a pseudoplastic behavior.

Structural, thermal, mechanical and viscoelastic properties of ethylene vinyl acetate (EVA)/olefin block copolymer (OBC) blends

In this study, ethylene vinyl acetate and olefin block copolymer (OBC) blends were prepared by melt-compounding. The effect of vinyl acetate (VA:12 and 28 wt%) and OBC (10–50 wt%) content on the morphological, thermal, and mechanical properties of EVA/OBC blends were studied in detail. Short-term flexural creep tests were also reported to investigate the time-dependent behavior of the blends. Non-isothermal crystallization results showed that, fractionated crystallization around 75C was observed in EVA (28%) blends. The creep study showed that the creep behavior of the blends significantly improves with the addition of OBC. The four-element Burgers model and the two parameter power law (Findley’s) model were fitted creep curves of the blends well. The addition of OBC promoted significant gains in terms of the mechanical and solid-state viscoelastic properties.

Effect of EVA copolymer containing different VA content on the thermal and rheological properties of bio-based high-density polyethylene/ethylene vinyl acetate blends

The effect of ethylene vinyl acetate (EVA) concentration and vinyl acetate (VA) content of EVA on the mechanical, morphological, and rheological properties of bio-based high-density polyethylene (BioPE)/EVA blends was investigated. The blends were characterized by X-ray diffraction, differential scanning calorimetry, scanning electron microscopy, and rheological measurements under oscillatory shear flow. The degree of crystallinity of BioPE decreased with the increase in the EVA concentration and was unaffected with the increase in the VA content. DMTA results showed a decrease in the storage modulus (E′) with the increase in EVA content and that the BioPE/EVA19 blends showed higher E′ values than BioPE/EVA28 blend. The impact strength substantially increased with the addition of EVA concentration above 5 mass% and was higher for the blends containing the highest VA content. The blends containing a higher content of VA exhibited the higher EVA dispersed phase domain size, which increased with the increase in EVA concentration. The complex viscosity increased with the increase in the EVA content, being higher for the BioPE/EVA blends containing higher VA content. The storage modulus increased, at low frequencies, with the increase in the EVA content and can be ascribed to the increase in the EVA dispersed phase domain size.

Preparation and properties of ethylene-vinyl acetate copolymer-based blend foams

In this study, ethylene-vinyl acetate (EVA) copolymer-based blend foams with polyolefin elastomers (POEs), low-density polyethylene, or styrenic thermoplastic elastomers were prepared as a potential resilient material for reducing inter-floor noise. Various properties of EVA blend foams were measured in order to reveal the effects of EVA content and types of pair polymers consisting of EVA blend foams on dynamic stiffness, which is one of the key factors of resilient materials, in relation to hardness, specific gravity, and resilience. These properties had not been introduced by the construction industry until now. When the EVA/POE ratio was 20/80 and the foaming ratio was 210%, dynamic stiffness presented the lowest value at 5.97 MN m− 3. However, when the resilience was <20%, dynamic stiffness was as high as 37.66 MN m− 3 at an expansion ratio of 210% even when the specific gravity was low.

Shape memory properties of polyethylene/ethylene vinyl acetate /carbon nanotube composites

The safe operation of electrical equipment relies on advanced polymer insulation to contain electrical pathways. Polymer sheath materials should be mechanically robust and chemically stable in order to protect the internal metal wiring from environmental attack. Polyethylene (PE) and ethylene vinyl acetate (EVA) have often been used as electrical cable jacket materials for electrical power industry. Partially crosslinked PE is able to shrink and wrap tightly around the metal wires upon stimulated by external heat, exhibiting shape memory behaviour. In this work, multiwalled carbon nanotubes (MWCNTs) were introduced to partially crosslinked linear medium density polyethylene (LMDPE) and EVA blend in order to enhance the shape memory performance at lower temperature by promoting the thermal transfer and antistatic properties of the polymer nanocomposite. The morphologies of the partially crosslinked and non-crosslinked composites are analysed. The MWCNTs preferentially resided in the EVA phase while the peroxide crosslinking process drastically altered the morphology and electrical properties. The addition of 3 wt% of MWCNTs resulted in a percolation transition and enhanced the alternating current (AC) conductivity by 10 orders of magnitude for non-crosslinked LMDPE/EVA and by 3 orders of magnitude for crosslinked LMDPE/EVA composites. LMDPE/EVA (80/20) containing 3 wt% MWCNTs possessed excellent shape recovery of 100% and shape fixing of 82%. The addition of MWCNTs can not only promote the shape memory efficiency of the polymer sheath material, but also introduce antistatic properties to avoid electrical shocking or sparking.

Influence of irradiation crosslinking on the flame‐retardant properties of polyolefin blends

ABSTRACTIn the presence of flame retardants and other additives, halogen‐free flame retardant (HFFR) shape‐memory polymers were prepared using blends of ethylene vinyl acetate, ethylene propylene diene monomer, and low‐density polyethylene. The HFFR compounds were irradiated using electron beam up to an absorbed dose of 150 kGy and characterized based on their mechanical, thermal, and electrical properties. Both the tensile strength (TS) and elongation at break (Eb) were found to increase as the levels of irradiation increased. This contrasted fact that, generally, Eb decreases as radiation doses increases because of polymer crosslinking capability. However, both TS and Eb decreased as the flame retardant content increased. The optimum mechanical properties were 13 MPa for TS and 200–350% for Eb. The versatile glass transition temperature greatly influenced the shape‐memory impact. Nevertheless, the variable rubbery modulus had no significant influence. The limiting oxygen index was found to increase as the total flame retardant contents increased to values over the range of 30–35%. Hardness was about 92, and the retentions of TS and Eb after thermal aging at 136 °C for 168 h were between 93–112 and 75–93%, respectively. UL94 ratings of V‐0 and a volume resistivity of 3.21 × 1015 to 3.49 × 1015 Ωcm were obtained using these HFFR compounds. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020, 137, 48649.

Rheology, Mechanical Properties and Morphology of Poly(lactic acid)/Ethylene Vinyl Acetate Blends

In this work, the effect of ethylene vinyl acetate (EVA) content on the rheology, mechanical properties, and morphology of poly (lactic acid) (PLA)/EVA blends was investigated. Differential Scanning Calorimetry (DSC) showed that the addition of EVA to PLA decreased the degree of crystallinity of PLA. Dynamic Mechanical Thermal Analysis (DMTA) results showed that the presence of EVA copolymer increased the cold crystallization temperature (Tcc) of PLA. The addition of 10% of EVA to PLA substantially increased the impact strength. Morphology analysis by Scanning Electron Microscopy (SEM) indicated the immiscibility between PLA and EVA phases and an in increase the EVA average dispersed phase domains size with the increase in EVA content. Rheological measurements under oscillatory shear flow showed that storage modulus (G′) increased with the increase in the EVA content at low frequencies and is related to the increase in the EVA dispersed phase domains size, as also observed by relaxation spectrum analysis. Cole–Cole plots of imaginary viscosity (η″) versus real viscosity (η′) and Han plots of storage modulus (G′) versus loss modulus (G″) indicated that PLA and EVA phases are immiscible, as also observed by SEM.

Shape Memory Properties of Melt-Blended Olefin Block Copolymer (OBC)/Ethylene-Vinyl Acetate Blends

The completely crosslinked shape memory polymer blends (SMPs) traditionally suffer from recycling problems due to their network structure. In this paper we describe the thermal, mechanical, and shape memory behavior of physical blends of OBC (Olefin block copolymer) and EVA (Ethylene-vinyl acetate copolymer), with and without modification of one or both of the components, prepared using a melt-blending method. These behaviors of the modified blends, based on maleated OBC (OBC-g-MA) and/or vinyltriethoxysilane (VTEOS) modified EVA, included OBC/EVA-g-VTEOS, OBC-g-MA/EVA, and OBC-g-MA/EVA-g-VTEOS blends; they were investigated to compare with the OBC/EVA blend. The SEM (scanning electron microscopy) observations showed that the compatibility of the silane and maleic anhydride modified OBC/EVA blends were better than that of the unmodified OBC/EVA blend. The crystallization temperatures of OBC and EVA in the modified blends were higher than those in the neat blend. The OBC-g-MA/EVA-g-VTEOS blend had the highest modulus and thermal stability of all investigated blend systems due to the numerous interactions between maleic anhydride and silane. The shape memory performance, as defined by the shape fixity ratio (Rf) and shape recovery ratio (Rr), was higher for the modified blends of one or both of the modified components than that for the OBC/EVA blend. These modified blends were readily reprocessible, like thermoplastic vulcanizates, and still retained shape memory behavior, in contrast with the fully crosslinked shape memory polymer blends; thus they were also improved in terms of the environmental aspects of processing.

The Effect of Nano Loading and Ultrasonic Compounding of EVA/LDPE/Nano-magnesium Hydroxide on Mechanical Properties and Distribution of Nano Particles

Blends of Ethylene Vinyl Acetate (EVA) and Low-Density Polyethylene (LDPE) are promising composite which have good mechanical properties to environmental stress cracking. However, they lack fire resistant properties, which limits it usage in wire and cable industry. In order to improve flame retardancy ability, a range of nano-magnesium hydroxide (nano-MH) loading which is from 0 phr to maximum of 20 phr with ultrasonic extrusion 0-100 kHz frequencies have been introduced. Ultrasonic extrusion was used to improve the distribution of nano-MH. It was found that, 10 phr of nano loading with 100 kHz ultrasonic assisted has greater tensile strength compared to the nanocomposite without ultrasonication. Further increase of nano MH loading, will decrease the tensile properties. Better elongation at break was observed at10 phr nano-MH with the frequency of 50 kHz. The sample of 20 phr of nanoMH assisted with 50 kHz ultrasonic exhibits good flexural properties while 10 phr of nano-MH without the ultrasonic assisted demonstrates good in izod impact properties. From the evaluation of mechanical properties studied, it was found that 10 phr of nano-MH has shown the best performance among all the samples tested for EVA/LDPE/nano-MH composites. Transmission Electron Microscopy (TEM) has been conducted on 10 phr sample with different frequencies in order to observe the distribution of nano-MH particles. The sample with 100 kHz frequency shows more uniform dispersion of nano-MH in EVA/LDPE composites. This investigation indicates that the ultrasonic technology can enhance the mechanical properties studied as well as the dispersion of nano particles in the composite.

Processing and properties of an ethylene–vinyl acetate blend foam incorporating ethylene–vinyl acetate and polyurethane waste foams

ABSTRACTWaste polyurethane foam (w‐PU) and waste ethylene–vinyl acetate foam (w‐EVA) were used as fillers for the production of an ethylene–vinyl acetate (EVA) blend foam. Two different foaming techniques (single‐stage and heat–chill processes) were used for this purpose. The waste foam concentration was varied up to 30 wt % of the original EVA. The physical, mechanical, and morphological properties of the filled foam were studied. The single‐stage process produced blend foams with a lower density and a greater cell size than the foams obtained by the heat–chill process. The density and compression strength of the blend foam increased as the percentage of w‐PU foam increased. However, for the w‐EVA/EVA blend foams, the addition of w‐EVA foam did not significantly affect the density or compression strength compared to the original EVA foams. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2017, 134, 44708.

Investigation on the Influence of EVA Content on the Mechanical and Thermal Characteristics of Poly(lactic acid) Blends

Poly(lactic acid) (PLA) has gained considerable attention nowadays as a biocompatible polymer owing to its advantage of being prepared from renewable resources. PLA exhibits excellent tensile strength, fabricability, thermal plasticity and biocompatibility properties comparable to many petroleum based plastics. However, low heat distortion temperature, brittleness and slow crystallization rate limit the practical applications of PLA. In order to address these limitations, an attempt has been made in the current work to prepare binary blends of PLA with ethylene vinyl acetate (EVA) at different compositions via melt mixing technique. Systematic investigation on the mechanical properties, thermal degradation and crystallization behavior for PLA-EVA blends was carried out. The impact strength of binary blends of PLA–EVA was found to increase significantly by 176% for 15 wt% of EVA compared to virgin PLA. This is due to the strong interfacial adhesion among PLA and EVA resulting in brittle to ductile transition. Scanning electron microscopy analysis for impact fractured surfaces of binary blends of PLA implied the toughening effect of PLA by EVA. Thermogravimetry analysis results revealed that the activation energy of PLA–EVA blends decreased with increase in EVA content in the PLA matrix. While, differential scanning calorimetry results obtained for PLA–EVA blends revealed the improvement in crystallinity when compared with neat PLA. The effect of EVA on non-isothermal melt crystallization kinetics of PLA was also examined via DSC at various heating rates. Decreasing trend in the t 1/2 values indicated the faster rate of crystallization mechanism after addition of EVA in the PLA matrix.

Preparation and characterization of EVA/PLA/sugarcane bagasse composites for water purification

Poly(lactic acid)/ethylene vinyl acetate blends and poly(lactic acid)/ethylene vinyl acetate/sugarcane bagasse composites were prepared by melt mixing. The lower viscosity of poly(lactic acid), the lower interfacial tension between poly(lactic acid) and sugarcane bagasse, and the wetting coefficient of poly(lactic acid)/sugarcane bagasse being larger than one, all suggested that sugarcane bagasse would preferably be in contact with poly(lactic acid). A fairly good dispersion of sugarcane bagasse was observed in the composites. Exposed fibre ends were observed in the composite micrographs, which were believed to add to the efficiency of metal adsorption. The impact properties depended more on the poly(lactic acid):ethylene vinyl acetate ratio than on the presence of sugarcane bagasse. The poly(lactic acid)/ethylene vinyl acetate blends showed two melting peaks at approximately the same temperatures as those of the neat polymers, which confirms the complete immiscibility of poly(lactic acid) and ethylene vinyl acetate at all the investigated compositions. Sugarcane bagasse-related weight loss occurred at higher temperatures for sugarcane bagasse in the composites, which could have been the result of the sugarcane bagasse being protected by the polymers, or a delay in the diffusion of the sugarcane bagasse decomposition products out of the sample. Water absorption increased with an increase in sugarcane bagasse loading in the composites. More lead was adsorbed than one would expect if the partial coverage of the fibre by the polymer is taken into account, and therefore it may be assumed that some of the lead was trapped inside the cavities in the composites and that the polymers may also have played a role in the metal complexation process, since both polymers have functional groups that could interact with the lead ions. The metal impurities underwent monolayer adsorption.

Multiresponsive Shape Memory Blends and Nanocomposites Based on Starch.

Smart multiresponsive bionanocomposites with both humidity- and thermally activated shape-memory effects, based on blends of ethylene-vinyl acetate (EVA) and thermoplastic starch (TPS) are designed. Thermo- and humidity-mechanical cyclic experiments are performed in order to demonstrate the humidity- as well as thermally activated shape memory properties of the starch-based materials. In particular, the induced-crystallization is used in order to thermally activate the EVA shape memory response. The shape memory results of both blends and their nanocomposites reflect the excellent ability to both humidity- and thermally activated recover of the initial shape with values higher than 80 and 90%, respectively.

Preparation and Performance Research of New High Toughness EVA Material

The blends of ethylene vinyl acetate (EVA) and thermoplastic polyurethane (TPU) were prepared by means of blending. The mechanical properties of EVA/TPU blends and thermal stability of the extrudates were investigated. The results show that the toughness of EVA/TPU has been improved after adding TPU into EVA, and doesn’t affect the thermal stability of material.

A Study on Physical Properties of Melt Blended Acrylonitrile Butadiene Styrene/Ethylene Vinyl Acetate Modified with Linear Low Density Polyethylene and Montmorillonite

ABSTRACTIn this study, acrylonitrile butadiene styrene/ethylene vinyl acetate-based melt blends were prepared using linear low-density polyethylene as modifier. Commercially available sodium montmorillonite clay was organically modified and incorporated in blends. Fourier transformed infrared was used to confirm the structure of the blend and composites. Morphology of acrylonitrile butadiene styrene / ethylene vinyl acetate blend showed two-phase structure that formed a well-aligned pattern with fine nanoclay distribution. Addition of organo-modified clay depicted increase in tensile strength (43%) and modulus (89%) in damage-free range. XRD results of sodium montmorillonite, organically modified Na-montmorillonite, and PNCs were compared to investigate the degree of dispersion in matrix.