Ethylene Octene Research Articles

Compression molding of ethylene–octene copolymer‐toughened polypropylene/graphene surfaces with actively controlled shape‐morphing microarchitectures induced by friction and wear

AbstractSuperhydrophobic microarchitectured polyolefin surfaces are currently used intensively in various industrial applications. However, the deployment of products made of these materials into practical application is typically constrained by their inferior dry sliding behaviors, which stem from their limited strength and toughness. To obtain reinforced and toughened superhydrophobic microstructured surfaces that can be easy to demold and overcome friction in the workplace, elastomeric ethylene–octene copolymer (POE) and rigid graphene (GP) were introduced into the polypropylene (PP) matrix to prepare microstructured PP/POE/GP surfaces by compression molding. The elongation at break is significantly improved by 2000% and reached up to 520.33%. The contact angle (CA) of the microstructured PP/POE/GP surface increases to 154.4°. They exhibit superhydrophobic and low adhesion characteristic, that is, lotus effect. The enhanced toughness of PP/POE/GP composites reduces wear debris and damage to microarchitecture during the abrasion process. Even after the microstructured PP/POE/GP surfaces were worn after a distance length of 3000 mm, they still exhibited superhydrophobic, but high adhesion characteristic, that is, petal effect. The controlled shape‐morphing microarchitectures formed on the microstructured PP/POE/GP surface abraded after 1000 mm, possessing wetting stability during droplet impacting.Highlights The elongation at break of composites was improved by 2000% through adding POE. The composite microstructure deforms to consume energy during abrasion and POE reinforces this energy dissipation process. POE improves fracture toughness and wetting stability of composites.

The all‐polymer composites and blends made of ethylene–octene copolymer and partially disentangled polypropylene using a new processing approach

AbstractAll‐polymer composites and blends of ethylene–octene copolymer (EOC) and polypropylene (PP) were produced in the extrusion process. They had the same composition (96:4 wt.%), but five different entanglement densities of PP macromolecules. Depending on the processing temperature, below or above the melting point of PP, fibers or spherical inclusions were formed inside the EOC matrix. The production of PP fibers directly during mixing was possible by reducing the entanglement of macromolecules in this polymer. During fiber formation by solid‐state plastic deformation, the crystallinity of PP decreased, especially for the less entangled polymers. The presence of fibers influenced the mechanical properties of the composites, which were different from those of the blends. Both in blends and composites, the matrix was reinforced, but in the composites the effect was stronger and the measured stresses increased with the lower degree of PP entanglement. SAXS and microscopic observations showed that cavitation occurred in the deformed composites. All‐polymer composites, in which the reinforcement was created as a result of polymer deformation with limited entanglements, have properties that are advantageously different from traditional ones, which opens the prospect of their application.

Fabrication of electrically conductive interconnected microcellular thermoplastic elastomeric foam composite for absorption dominating electromagnetic interference shielding with ultra low reflection

AbstractThe elevated rates of electromagnetic radiation pollution, resulting from the growing need for wireless communication systems and electronic gadgets, have sparked interest in creating shielding materials that are lightweight, flexible, non‐corrosive, simply processable, and affordable. In this study, a collection of microcellular nanocomposites based on ethylene octane copolymer (EOC) were created utilizing Vulcan XC 72 conductive carbon black (VCB) by a dual mixing process involving both melt and solution mixing. A chemical blowing agent was utilized to induce the cellular architecture in the composite, resulting in its lightweight nature (maximum density of 0.65 g/cc). The composite foam, when loaded with 30 parts per hundred of volume (phr) of VCB, displays a conductive network and also achieves an electromagnetic interference (EMI) shielding efficiency of 23.2 decibels (dB), satisfying commercial requirements. Furthermore, the findings indicated that the composite's cellular structure significantly influences the absorption‐dominated EMI shielding mechanism with an absorption rate of 89%–94% and a specific shielding effectiveness of 194 dBcm2/g within the frequency range of 8.2–12.4 GHz (X band). The foam composite also demonstrated as a thermal management system, with a maximum thermal conductivity of 0.3 W/mK. As a result, this lightweight, easily processable, electrical conductive EOC/VCB polymer composite foams are projected to be used as EMI shielding materials in electronics, cars, and packaging.Highlights Fabrication of lightweight microcellular Carbon black‐loaded EOC composite Rheological, mechanical, and thermal properties of foam composites The cell density filled composites reduces by the cellular foam structures Carbon black pronouncedly enhanced the electrical conductivity of foam composite An absorption‐dominated shielding effectiveness with ultra‐low reflection.

Dielectric Breakdown Strength of Polypropylene Blended with Ethylene Octene Elastomers

Polymer blends have become a major focus of research in exploring the potential for new dielectric material applications, particularly in the insulation of high voltage systems. In the current research area, polypropylene (PP) is being investigated as an insulation material for high voltage alternating current and direct current power cables. However, PP must be treated with rubbery materials such as elastomers to lessen its overall stiffness for power cable extrusion. While various promising results have been published on the potential use of PP/elastomer blends as dielectric materials, the dielectric effects of adding ethylene octene elastomer to PP have been less explored. This paper discusses the alternating current (AC) and direct current (DC) breakdown strength of PP that contains different amounts of ethylene octene elastomer (10, 30, and 50 wt%). The addition of ethylene octene elastomer to PP affects the breakdown performance of the blend systems under both AC and DC fields. Significantly, an increase in elastomer contents results in a notable reduction in the AC and DC breakdown strength. A discussion is presented on the mechanisms underlying the change in the breakdown strength caused by the different amounts of ethylene octene elastomer blended with PP.

Thermo-Responsive Shape Memory Thermoplastic Elastomer Based on Natural Rubber and Ethylene Octene Copolymer Blends

The shape memory (SM) polymers with superior SM properties were successfully fabricated based on melt blending of natural rubber (NR) and ethylene octene copolymer (EOC) at various crystallinity of EOC phase. The differential scanning calorimetry analysis, mechanical properties, temperature scanning stress relaxation, and shape memory properties were studied. Results revealed that the mechanical and thermal properties of the prepared NR/EOC blends improved as a function of amount of ethylene fraction in the EOC phase. The ethylene segment of EOC in the NR/EOC blend is triggered as a stimulus-sensitive domain. The shape memory properties in terms of shape fixity and shape recovery efficiencies of the blends tended to increase with the increasing of crystalline segments in the blends. The shape memory properties of the prepared blends substantially exceed the best performance (close to 100%) by blending the NR/EOC at 50/50 parts by weight, having 62%–80% of ethylene content in the EOC phase, which corresponds to approximately 3°–16° of crystallinity of EOC phase in the blends.

Correlation of morphology, rheology, thermal, and mechanical properties in PP/EOC blends in presence of nanoclay and compatibilizer

ABSTRACT To expand the range of applications and overcome mechanical limitations of Polypropylene (PP), a commonly used industrial polymer, toughness modification is required. In this study, PP was toughened with ethylene octene copolymer (EOC) and nanoclay platelets and the blends and nanocomposites of PP/EOC were prepared by means of a melt mixing process, and the effect of different grades of EOC, the addition of nanoclay platelets, and the effect of compatibilizer on properties of the final system were investigated. Scanning and transition electron microscopy, X-ray diffraction, rheology, differential scanning calorimetry, and dynamic-mechanical analysis were conducted to correlate the structure to the resulting properties. The results indicate that different grades of EOC with different molecular weights and viscosity can have a tremendous impact on droplet size and final properties of the blend sample. From a morphological point of view, the addition of EOC grade with higher viscosity (ƞi) in PP/EOC blends results in droplet matrix structure with larger EOC droplets. To decrease the droplet size, and hence improvement in final properties, nanoclay and compatibilizer were introduced to the blend. According to the results, selective localization of nanoclay and proper dispersion degree of nanoclay in the PP/EOC blend with higher viscosity grade of EOC containing nanoclay up to 3 wt.% lead to amelioration of the final properties of the system including complex viscosity, storage modulus, damping, and crystallinity. Moreover, the addition of the compatibilizer to the nanocomposite samples with 5 wt.% nanoclay can compensate for the deteriorated properties which occurred as a result of nanoclay aggregation in this system. This indicates that the addition of the nanoclay and compatibilizer plays an important role in toughening, morphology, and determining the final properties of the system as well.

Toward understanding the crystallization behavior of polypropylene‐based nanocomposites: Effect of ethylene–octene copolymer and nanoclay localization

AbstractThe crystallization properties of polypropylene (PP), a widely used polymer in industry, can be modified to overcome its mechanical limitations. In the current work, we investigated the effect of ethylene octene copolymer (EOC), blend morphology, nanoclay loading, nano‐localization, and component ratios on PP/EOC crystallization behavior in various aspects, including crystallization rate, degree of crystallinity, nucleation state, and crystalline phases. The results revealed that adding EOC with varying ratios can decrease PP crystallinity both in degree and rate due to the partial miscibility of components through grafting. Furthermore, it was found that the effect of the nanoclay on the crystallization behavior of PP is dependent on the nanoclay loading and its localization in the blend. The nanoclay, therefore, served as a nucleation agent at low nanoparticle contents, accelerating the crystallization rate regardless of the blend's microstructure. However, the crystallization rate of the blend samples at high nanoclay contents (above the rheological percolation threshold) was strongly influenced by the type of morphology. Accordingly, high nanoclay concentrations in blends with matrix‐dispersed morphologies reduced crystallization rates (increasing half‐time from 164 to 216 and 186 s), primarily because PP chains slowed down due to their interactions with nanoparticles and nanoclay hindrance. In contrast, in a blend with a co‐continues‐type morphology, the crystallization rates increased (decreasing half‐time from 624 to 270 and 236 s) due to nano‐localization at the interface and morphology transformation to the matrix‐dispersed one. The blends and nanocomposites based on PP/EOC were also investigated to determine the relationship between the crystallization behavior and mechanical properties.

Elastic Electrically Conductive Composites Based on Vapor-Grown Carbon Fibers for Use in Sensors.

Elastic electrically conductive composites with an ethylene octene copolymer matrix (EOC) and vapor-grown carbon fibers (VGCF) were prepared by ultrasonication in a toluene solution, and their morphology, mechanical and electrical properties were also evaluated. EOC/CF composites were estimated for their mechanical and viscoelastic properties. The morphology of the composites was analyzed using scanning electron microscopy (SEM), and stress-strain curves were generated to measure the stress and tensile modulus of the composites. The experimental results were compared with various theoretical models, including the Burgers model, which separates viscoelastic behavior into several components. A dynamic mechanical analysis was also used to measure the composites' storage modulus, loss modulus, and damping factor at different frequencies. The composites' complex viscosity and storage modulus were increased with higher wt.% of CF, which enhances the elastic response. Electrical resistivity measurements were conducted on the composites and it was found that the resistivity decreased as the sample was loaded and increased as it was unloaded. Overall, the study provides insights into the mechanical and viscoelastic properties of EOC/CF composites, which could be helpful in developing sensors such as pressure/strain sensors.

Self-healing and wear resistance stable superhydrophobic composite coating with electrothermal and photothermal effects for anti-icing

Superhydrophobic material has great potential applications in the field of anti-icing due to its special wettability. However, the poor wear resistance of the material has restricted its practical applications. Based on this, a simple two-step spray method was used to prepare a self-healing and robust superhydrophobic coating with excellent photothermal/electrothermal effect for anti-icing using epoxy modified ethylene octene copolymer (POEG) resin as the substrate layer and the fluorinated carbon black as the top coating. Results showed that the obtained composite coating showed multi-level rough structure and possessed excellent superhydrophobicity toward water droplets with different pH. Meanwhile, the composite coating could resist abrasion and kept superhydropbobicity even 250 cycles abrasion test with a water contact angle higher than 150o. When the surface was subjected to the intense abrasion, the rough structure and the superhydrophobic property of the surface were destroyed. However, it could be restored by the abrasion of the rougher surface. In addition, the scratches on the surface could be completely repaired by the heat treatment, indicating the good self-healing performance of the composite coating. Due to the existence of the carbon black particles, the superhydrophobic coating had good photothermal/electrothermal effects, which endowed the surface with excellent anti-icing performance of removing the icing under the conditions of electrothermal and light. This paper provides a simple and convenient way to prepare functional self-healing superhydrophobic coating, and a new idea for the preparation of anti-icing coating.

Crystallization, Phase and Mechanical Behaviors of Linear Low Density Polyethylene/Thermoplastic Polyolefin Elastomer Blends

Blending polyethylene with thermoplastic polyolefin elastomers (TPOs) is a promising way to manipulate its structures and tailor its properties. Herein, three TPOs, i.e., two ethylene–octene copolymers (EOCs) and an olefin block copolymer (OBC) with different structures, were used to comparatively investigate the miscibility, crystallization, and phase behavior of their blends with a linear low-density polyethylene (LLDPE). It was found that large differences occurred in the crystallization and phase behaviors of the blends due to the different extent of similarity in the molecular structure between the TPO and the LLDPE matrix. In particular, a unique segregated phase morphology comprised a less stable crystalline phase and a rubbery phase was found in an LLDPE/EOC blend. The tensile performance and elasticity of the blends were also studied and correlated with the structures of the blends. This work not only provides novel results on the miscibility and phase behavior of the similar-structured LLDPE/TPO blends, but can also guide the design of LLDPE-based products with tailored performances.

Enhancement of Mechanical Properties of High Melt Flow Polypropylene & Ethylene - Octene Copolymer Blends

In this current study, we have investigated and compared the improvement on the mechanical properties of high melt flow polypropylene copolymer (PPCP1) and ethylene-based α-olefin elastomer i.e. Polyolefin elastomer by incorporating intermediate melt flow index polypropylene copolymer (PPCP2IF) and changing the composition of ethylene octene impact modifier (E.O1 & E.O1/ E.O2/ HDPE) while keeping the matrix copolymer (PPCP1) as such. This paper reports the experimental issues associated with data measurement, and a procedure for determining properties by modeling and extrapolation is proposed. Impact modifiers explored are olefinic copolymers i.e. ethylene - octene elastomer having different melt flow index of, 5 gm/10 min (EO1) and ethylene - octene elastomer of 0.5 gm/10 min (EO2). The inclusive performance of high melt flow polypropylene (PPCP1) - EO1 & high melt flow polypropylene (PPCP1) - (E.O1/ E.O2/ HDPE) blends are compared in terms of various mechanical and rheological properties by varying intermediate M.F.I. PPCP (PPCP2IF) content from 0% - 20%. Results shows that at low PPCP2IF content (<10%), the intensification in impact strength is insignificant while extra high toughness observed in the range of 10% - 20 % PPCP2IF when added to PPCP1 & E.O1/ E.O2/ HDPE system . Presence of HDPE plays a huge role in preventing coalescence of the rubber particles leading to better and finer dispersion of the rubber particles. Our research will give a new combination of PPCP and POE blends for perfect balance of toughness and stiffness which is a very essential requirement for automotive TPO application

Effect of multi‐walled carbon nanotube localization on toughening mechanism and electrical properties of compatibilized PP/EOC immiscible blend

AbstractToughness modification of polypropylene (PP), a widely used polymer in industry, is an important factor in overcoming mechanical limitations and extending its scope of application. In the present work, we utilized a combination of nanoparticle and elastomer techniques to enhance the toughness of PP. Accordingly, the nanocomposite blends, including PP, ethylene octene copolymer (EOC), and multi‐walled carbon nanotubes (MWCNTs), were prepared through three different feeding methods (direct, sequential, and masterbatch). The results demonstrated that the different feeding methods significantly affect the localization and dispersion degree of the MWCNTs, and hence, toughness modification. The results also showed that the sequential is the most effective method to prepare the nanocomposites with the reinforced fracture toughness so that the addition of 2 phr MWCNTs to the PP/EOC blend leads to a high impact strength (=351.61 J/m). Because in this feeding method, most of the highly dispersed MWCNTs can be selectively located in the EOC particles as well as the interface, which can not only intensify the interfacial interactions between the two phases but also help the stress transfer and superposition of stress fields. Moreover, it was shown that in the sequential method, the MWCNTs could facilitate the creation of electrically conductive pathways as a result of nanoparticle bridging and the formation of an interconnected percolating network, therefore increasing the electrical properties.

Effects of core‐shell structured rubber on biobased polyamide 56 with stiffness and toughness balance

AbstractThere is great social awareness concerning the use of biobased materials of diminishing the rapid resource depletion and suppressing global warming. The inherent drawbacks of biobased polyamide 56 (PA56) such as poor notched impact strength limit its applications. Core‐shell structured impact modifiers consisting of a soft glycidyl methacrylate grafted poly(ethylene–octene) (POE‐g‐GMA) shell and a rigid polypropylene core were synthesized through the differences in interfacial tensions. Core‐shell rubber (CSR) particles were used to toughen biobased PA56 by melt blending. PA56/CSR composites exhibited a 560% increase in the impact strength, while the tensile performance loss was slight. This desirable toughness of biobased PA56 is attributed to the cavitation that occurred in POE‐g‐GMA shell which can induce shear bands and shear yielding, forming the fibrils. Characterizations, including X‐ray diffraction (XRD), differential scanning calorimetry (DSC), scanning electron microscopy (SEM), melt rheological tests, and dynamic mechanical analysis (DMA) were conducted to study the toughening mechanism. The results indicated the massive shearing yielding, the cavitation of the CSR and interfacial debonding between the POE‐g‐GMA and the PP were the principal toughening mechanisms.

Flexible Encapsulation and Module of Thin‐Film GaInP/GaAs/InGaAs Solar Cells

Lightweight and flexible III–V solar cells create new opportunities for application in satellites, drones, and wearable devices. In this article, a module manufacturing scheme based on resistance welding and lamination technology is proposed to meet the demands of practical application. A combined laminate structure of ethylene–tetrafluoroethylene plus ethylene octene copolymer and polyimide is used to encapsulate flexible III–V solar cells. In laboratory measurements with a spectrum close to AM1.5G, the photoelectric conversion efficiency of the flexible solar cell is 34.4% with an open‐circuit voltage of 3.04 V, and the efficiency of the flexible module is 32.7% with a weight density of 469 g m−2. The electroluminescence measurements show good performance of the flexible solar cell module, which is expected to achieve large‐size flexible III–V solar cells encapsulation.

Rheology, crystallization, and enhanced mechanical properties of uniaxially oriented ethylene–octene copolymer/polyolefin elastomer blends

The application of polyethylene in artificial turf promotes research on the processing and properties of uniaxial extension modified polyethylene materials. The effects of comonomer (octene/butene) structure on the properties of pre-stretched linear low density polyethylene (LLDPE)/polyolefin elastomer (POE) blends are investigated. The melt tensile stress and melt stretch ratio of LLDPE ethylene‒octene copolymer (EOC)/POE reach 4.0 × 105 Pa and 12.8, respectively. At the pre-stretching ratio λ = 5, the tensile strength of EOC/POEλ5 reaches 62.5 MPa, the critical length is 5.7 mm, and the strain hardening degree increases. Differential scanning calorimetry, Raman spectroscopy and X-ray diffraction show the crystallinity of EOC/POEλ5 is higher than that of LLDPE ethylene‒butene copolymer (EBC)/POEλ5. Large short-chain branch length EOC is demonstrated to rebuild the “physical crosslinking point” after pre-stretched, thereby enhancing the interaction between molecular chains in EOC/POEλ5. This research provides a new clue for the development of artificial turf materials.

Thermoplastic Elastomer based on Recycled HDPE/Ground Tire Rubber Interfacially Modified with an Elastomer: Effect of Mixing Sequence and Elastomer Type/Content

ABSTRACT The effect of interfacial interaction and processing methods (one-step and two-step) on the structure–property relationships of ternary blends was investigated. The addition of ethylene-vinyl acetate (EVA) and ethylene octene copolymer (POE) resulted in homogeneous structure and greatly improved rubber-like properties of recycled high-density polyethylene (rHDPE) and regenerated tire rubber (RR) blends. Interfacial tension calculations revealed a high tendency of POE to encapsulate rubber particles (complete wetting). The two-step processing contributed to perfect encapsulation of the rubber phase via a soft/thick POE interface resulting in uniform RR particle dispersion, high elongation at break (138.5%), and impact strength (394 J/m) of rHDPE/(RR/POE) (20/80) ternary blend.

Reactive processing of poly(lactic acid)/poly(ethylene octene) blend film with tailored interfacial intermolecular entanglement and toughening mechanism

In order to obtain a uniform and effectively toughened poly (lactic acid) film by blending with low content of poly (ethylene octene) (POE) with high elasticity, the tailored interfacial intermolecular interaction and entanglement between the two phases of the PLA/POE blend was innovatively constructed via the facile reactive melt blending process through the reaction of the epoxy/anhydride groups grafted on the POE chains with the end groups of PLA chains (PLA/GPOE-MPOE). It was observed that POE domains were embedded tightly in PLA matrix with a fuzzy interface and abundant interface transition area, and the impact fractured surface of the blend showed an obvious plastic deformation with less occurrence of fibrillation of PLA matrix or interfacial de-bonding. Compared with neat PLA and directly blended PLA/POE blends, the PLA/GPOE-MPOE blend exhibited much higher complex viscosity/storage modulus, much lower tanδ values in the terminal region, and obvious strain-hardening behavior. The deviation in viscoelastic behavior of PLA/GPOE-MPOE from linear PLA indicated the enhanced molecular entanglement between the long-branched chains, resulting in an enhancement of the stretching ability during biaxial drawing of the blend. Uniform PLA/GPOE-MPOE films with draw ratio as high as 7 × 7 were obtained through biaxial stretching, which showed much higher tensile strength and the elongation at break than that of neat PLA and PLA/POE film. This work provides a facile method for fabricating toughening PLA films with application potentials.

Production of Eco-Sustainable Materials: Compatibilizing Action in Poly (Lactic Acid)/High-Density Biopolyethylene Bioblends

Motivated by environment preservation, the increased use of eco-friendly materials such as biodegradable polymers and biopolymers has raised the interest of researchers and the polymer industry. In this approach, this work aimed to produce bioblends using poly (lactic acid) (PLA) and high-density biopolyethylene (BioPE); due to the low compatibility between these polymers, this work evaluated the additional influence of the compatibilizing agents: poly (ethylene octene) and ethylene elastomer grafted with glycidyl methacrylate (POE-g-GMA and EE-g-GMA, respectively), polyethylene grafted with maleic anhydride (PE-g-MA), polyethylene grafted with acrylic acid (PE-g-AA) and the block copolymer styrene (ethylene-butylene)-styrene grafted with maleic anhydride (SEBS-g-MA) to the thermal, mechanical, thermomechanical, wettability and morphological properties of PLA/BioPE. Upon the compatibilizing agents’ addition, there was an increase in the degree of crystallinity observed by DSC (2.3–7.6% related to PLA), in the thermal stability as verified by TG (6–15 °C for TD10%, 6–11 °C TD50% and 112–121 °C for TD99.9% compared to PLA) and in the mechanical properties such as elongation at break (with more expressive values for the addition of POE-g-GMA and SEBS-g-MA, 9 and 10%, respectively), tensile strength (6–19% increase compared to PLA/BioPE bioblend) and a significant increase in impact strength, with evidence of plastic deformation as observed through SEM, promoted by the PLA/ BioPE phases improvement. Based on the gathered data, the added compatibilizers provided higher performing PLA/BioPE. The POE-g-GMA compatibilizer was considered to provide the best properties in relation to the PLA/BioPE bioblend, as well as the PLA matrix, mainly in relation to impact strength, with an increase of approximately 133 and 100% in relation to PLA and PLA/BioPE bioblend, respectively. Therefore, new ecological materials can be manufactured, aiming at benefits for the environment and society, contributing to sustainable development and stimulating the consumption of eco-products.

The Modulus of the Amorphous Phase of Semicrystalline Polymers

A universal method for determining the modulus of the interlamellar amorphous phase of semicrystalline polymers was proposed. The basics of the method were presented on the example of high-density polyethylene (HDPE). The local deformation of the amorphous component was induced by the introduction of a swelling agent (hexane). The swelling-induced local strain and local stress of the interlamellar amorphous phase were estimated based on the changes of the long period and the yield stress, respectively. The determined modulus of the interlamellar amorphous phase of HDPE (≈40 MPa) was an order of magnitude higher than the modulus of the bulk rubbery amorphous phase of HDPE (≈3 MPa). The modulus of the interlamellar amorphous phase of other semicrystalline polymers, such as polypropylene (PP), low-density polyethylene (LDPE), and an ethylene–octane copolymer (EOC), was also determined and amounted to 50.3, 11.8, and 4.2 MPa, respectively. For polyethylene materials (HDPE, LDPE, and the EOC), a linear increase in the modulus of the interlamellar amorphous phase with increasing of the degree of crystallinity was observed. This effect was correlated with a decrease in “deformability” of the amorphous layers (a decrease in the swelling-induced local strain of amorphous layers for samples with higher crystallinity). The decrease in “deformability” of the amorphous component at low strains was probably caused by an increase in the density of stress transmitters (entanglements and tie molecules), which affected the mechanical properties (modulus) of the interlamellar regions. In the case of the material with the lowest degree of crystallinity (EOC, 26.2 vol%), the modulus of the interlamellar amorphous phase was similar to the modulus of the bulk rubbery amorphous phase, which indicated a very limited influence of the lamellar crystals on the stiffness of the amorphous regions.

Effect of glycidyl methacrylate-grafted poly(ethylene octene) on the compatibility in PLA/PBAT blends and films

Effect of glycidyl methacrylate-grafted poly(ethylene octene) on the compatibility in PLA/PBAT blends and films