Copolymer Blends Research Articles

Enhanced hydrophilicity of low melting point polylactic acid by butenediol vinyl alcohol copolymer via melt blending

In order to solve the poor hydrophilicity of low melting point polylactic acid (LMPLA) limiting its application in absorbent sanitary products. LMPLA/butenediol vinyl alcohol copolymer (BVOH) blends with different ratios were manufactured by simple melt blending. The BVOH exhibited good compatibility and dispersity in LMPLA matrix without chemical reaction, and LMPLA/BVOH blends showed sea-island structure. The introduction of BVOH could promote the crystallization of LMPLA and improve the crystallinity, whereas the crystallization of BVOH were limited. Furthermore, the introduction of BVOH could also decrease the thermal stability of LMPLA without affecting its application, but the tensile stress of LMPLA could be significantly increased. The tensile stress of LMPLA/BVOH blends could reach 78.59 MPa (increased by 10.9%) when he BVOH content was 3 wt%. Most importantly, the introduction of BVOH could significantly improve the hydrophilicity of LMPLA. The initial water contact angle decreased from 68.5° to 51.4° with the increase of BVOH content, and the contact angle decreased from 63.7° to 44.6° at 60 s. Moreover, the contact angle change rate of LMPLA/BVOH blends increased with the increase of BVOH content at different contact time, which also indicated adding BVOH could sharply improve the hydrophilicity of LMPLA.

Biological, anti-inflammatory and antioxidant activity of c-PEI based silica nano composites

In this study, a mixed sol-gel technique using silicate, polyvinyl alcohol (PVA), and polyethyleneimine (PEI) was used to various polymers based on PEI and silica gel. The c-PEI blend co-polymer was synthesized by cross-linking branching PEI in an aqueous solution with PVA. The produced c-PEI particles were highly positively charged and fit inside the range of tens to hundreds of nanometers of silica gel. It has been shown that the prepared c-PEI nanocomposite is a very effective antimicrobial, anti-inflammatory, and antioxidant material. In addition to the appropriate investigation of the anti-inflammatory activity using human red blood cells (HRBCs) stabilization, the developed materials were used to explore antimicrobial activity against yeast (Candida albicans ATCC-10231), Gram-negative bacterial strain (Escherichia coli ATCC-25922), and Aspergillus niger NRRL-3 as a fungus. FTIR, XRD, TEM, TGA, and DSC were among the biological and chemical methods used to characterize the produced c-PEI nanocomposites. The agar diffusion method was used to assess the biological activity of the synthesized compounds, and the results revealed a range in their in vitro-antimicrobial inhibitory activity. Based on the type of pathogenic microbe, the majority of the test substances showed a wide range of activity. The examined substances may be appropriate for the creation of an innovative antibacterial and antifungal medicinal medication.

Stretchable semiconducting triblock copolymer blends: Exploring the impact of block size

Stretchable semiconductors are vital for the development of emerging electronic biointerfaces. The physical blending of polymer semiconductors into elastomers presents a promising and straightforward method for creating stretchable films with high charge carrier mobilities. However, the understanding of the interplay between film morphology and the associated mechanical and electronic characteristics in blends is still limited. Especially, investigations into the blending behavior of more complex conjugated polymers, such as block copolymers, are lacking. In this study, we investigate the blending behavior of two semiconducting and stretchable triblock copolymers (TBCs). These copolymers comprise a middle block of poly(diketopyrrolopyrrole-co-thienothiophene) (PDPP-TT) and two outer blocks of poly(dimethylsiloxane) (PDMS) with different block-size ratios (85:15 and 40:60). The TBCs are blended into a crosslinked PDMS matrix. The resulting blends exhibit superior stretchability compared to the PDPP-TT homopolymer and retain their electric properties down to 40% PDPP-TT content in the blend. Increasing the PDMS block size inhibits macrophase separation and results in drastic decrease in charge carrier mobility, suggesting the necessity for macrophase separation within TBC/elastomer blends to maintain superior electric properties.

Mesoporous silica nanoparticles accommodating electrospun nanofibers as implantable local drug delivery system processed by cold atmospheric plasma and spin coating approaches

Nanofibers (NF) and nanoparticles are attractive for drug delivery to improve the drug bioavailability and administration. Easy manipulation of NF as macroscopic bulk material give rise to potential usages as implantable local drug delivery systems (LLDS) to overcome the failures of systemic drug delivery systems such as unmet personalized needs, side effects, suboptimal dosage. In this study, poly(ethylene glycol) polyethyleneimine (mPEG:PEI) copolymer blended poly ϵ-caprolactone NFs, NFblend accommodating mesoporous silica nanoparticles (MSN) as the implantable LLDS was achieved by employing spin coating and cold atmospheric plasma (CAP) as the post-process for accommodation on NFblend. The macroporous morphology, mechanical properties, wettability, and in vitro cytocompatibility of NFblend ensured their potential as an implantable LLDS and superior features compared to neat NF. The electron microscopy images affirmed of NFblend random fiber (average diameter 832 ± 321 nm) alignments and accessible macropores before and after MSN@Cur accommodation. The blending of polymers improved the elongation of NF and the tensile strength which is attributed as beneficial for implantable LLDS. CAP treatment could significantly improve the wettability of NF observed by the contact angle changes from ∼126° to ∼50° which is critical for the accommodation of curcumin-loaded MSN (MSN@Cur) and in vitro cytocompatibility of NF. The combined CAP and spin coating as the post-processes was employed for accommodating MSN@Cur on NFblend without interfering with the electrospinning process. The post-processing aided fine-tuning of curcumin dosing (∼3 µg to ∼15 µg) per dose unit and sustained zero-order drug release profile could be achieved. Introducing of MSN@Cur to cells via LLDS promoted the cell proliferation compared to MSN@Cur suspension treatments and assigned as the elimination of adverse effects by nanocarriers by the dosage form integration. All in all, NFblend-MSN@Cur was shown to have high potential to be employed as an implantable LLDS. To the best of our knowledge, this is the first study in which mPEG:PEI copolymer blend NF are united with CAP and spin coating for accommodating nano-drug carriers, which allows for NF both tissue engineering and drug delivery applications.

Phase behavior of triblock copolymer and homopolymer blends: Effect of copolymer topology

Two distinct linear triblock copolymers with different block sequences, ABA or BAB, are obtained when two identical AB diblock copolymers are jointed at their B or A ends, respectively, resulting in three homologous, AB diblock, ABA, and BAB triblock copolymers with the same chemical composition but different topologies. We demonstrate that the topological effect on the phase behaviors of these copolymers is amplified when A homopolymers are added to the system. Specifically, the phase behaviors of binary blends composed of ABA or BAB linear triblock copolymers and A homopolymers are studied by using the random-phase approximation (RPA) and self-consistent field theory (SCFT). The RPA analysis predicts that the Lifshitz point for the ABA/A blends behaves like a second-order transition but that for the BAB/A blends behaves like a first-order transition. The Lifshitz point of the BAB/A mixtures is found to occur at a much lower homopolymer concentration than that of the ABA/A mixtures, indicating a poorer miscibility of the A homopolymers into the BAB than ABA triblocks, which is also confirmed by SCFT. For sphere-forming triblock copolymers mixed with homopolymers, the poorer miscibility and the more diffused distribution of the A homopolymers in the BAB/A blends result in a phase behavior drastically different from that of the ABA/A and AB/A blends. The ABA/A blends stabilize the Frank-Kasper (FK) phases similar to the AB/A blends, but the stability window of FK phases becomes negligibly small in the corresponding BAB/A blends. Our results demonstrate that the topological effect of block copolymers on the equilibrium phase behaviors can be more prominent in multicomponent systems and thus more attention should be paid to copolymer topologies in the design of polymeric blends. Published by the American Physical Society 2024

Bicontinuous microemulsion in binary blends of complementary diblock copolymers.

The phase behavior of binary blends of AB diblock copolymers of compositions f and 1 - f is examined using field-theoretic simulations. Highly asymmetric compositions (i.e., f ≈ 0) behave like homopolymer blends macrophase separating into coexisting A- and B-rich phases as the segregation is increased, whereas more symmetric diblocks (i.e., f ≈ 0.5) microphase separate into an ordered lamellar phase. In self-consistent field theory, these behaviors are separated by a Lifshitz critical point at f = 0.2113. However, its lower critical dimension is believed to be four, which implies that the Lifshitz point should be destroyed by fluctuations. Consistent with this, it is found to transform into a tricritical point. Furthermore, the highly swollen lamellar phase near the mean-field Lifshitz point disorders into a bicontinuous microemulsion (BμE), consisting of large interpenetrating A- and B-rich microdomains. BμE has been previously reported in ternary blends of AB diblock copolymer with its parent A- and B-type homopolymers, but in that system the homopolymers have a tendency to macrophase separate. Our alternative system for creating BμE is free of this macrophase separation.

An exploration of novel natural gas leak detection based on the efficient CH4/N2 separation of polymer blend membrane

The CH4/N2 high-efficiency membrane separation technology is capable of effectively enriching CH4 from natural gas, and holds great potential for application in the fields of biogas purification and natural gas pipeline leak detection. However, preparing high-performance separation membranes is challenging due to the similarity between CH4 and N2 molecules. To enhance the CH4/N2 separation performance, block polyetheramide copolymer (Pebax)/EVA blended membranes were fabricated in this study. Additionally, a novel gas leakage detection tube was prepared. The EVA14 (14 wt% VA) membrane exhibits an optimal transport-facilitated channel among a series of pure EVA membranes, resulting in a CH4 permeability of 21.41 Barrer and CH4/N2 selectivity reaches 1.80 under mixed-gas feed conditions at 35 °C. The CH4 permeability of Pebax/EVA (30 wt%) reaches 120.5 Barrer by physical blending, and the CH4 permeability is increased by 191 % in comparison with pure EVA14 membrane. The Pebax/EVA (10 wt%) membrane exhibits the optimum CH4/N2 selectivity, and compared with pure EVA membrane increased by 35.5 %. EVA and Pebax polymers are blended for the first time for CH4/N2 separation, and the blending of block polyetheramide copolymer intensifies the membrane's separation performance comprehensively. The natural gas leak detection tube was fabricated with a membrane, offering a new and efficient CH4/N2 separation strategy.

Using Redox-Switchable Polymerization Catalysis to Synthesize a Chemically Recyclable Thermoplastic Elastomer.

In an effort to synthesize chemically recyclable thermoplastic elastomers, a redox-switchable catalytic system was developed to synthesize triblock copolymers containing stiff poly(lactic acid) (PLA) end blocks and a flexible poly(tetrahydrofuran-co-cyclohexene oxide) (poly(THF-co-CHO) copolymer as the mid-block. The orthogonal reactivity induced by changing the oxidation state of the iron-based catalyst enabled the synthesis of the triblock copolymers in a single reaction flask from a mixture of monomers. The triblock copolymers demonstrated improved flexibility compared to poly(l-lactic acid) (PLLA) and thermomechanical properties that resemble thermoplastic elastomers, including a rubbery plateau in the range of -60 to 40 °C. The triblock copolymers containing a higher percentage of THF versus CHO were more flexible, and a blend of triblock copolymers containing PLLA and poly(d-lactic acid) (PDLA) end-blocks resulted in a stereocomplex that further increased polymer flexibility. Besides the low cost of lactide and THF, the sustainability of this new class of triblock copolymers was also supported by their depolymerization, which was achieved by exposing the copolymers sequentially to FeCl3 and ZnCl2 /PEG under reactive distillation conditions.

Reaction-induced morphological transitions in a blend of diblock copolymers and reactive monomers: dissipative particle dynamics simulation.

The dissipative particle dynamics (DPD) method is applied to the morphological transitions of microphase-separated domains in a mixture of symmetric AB-diblock copolymers and reactive C-monomers, where polymerization and cross-linking reactions take place among C-monomers. The initial structure for the DPD simulation is an equilibrated cylindrical domain structure prepared by the density-biased Monte Carlo method with density profiles obtained from the self-consistent field theory. By introducing a cross-linking reaction among reactive C-monomers, we confirmed that the DPD simulation reproduces the morphological transitions observed in experiments, where the domain morphology changes due to segregation between A-blocks of diblock copolymers and cross-linking networks of C-monomers. When the cross-linking reaction of C-monomers is sufficiently fast compared to the deformation of the domains, the initial cylindrical domains are preserved, while the distance between the domains increases. On the other hand, when the formation of the cross-linking network is slow, the domains can deform and reconnect with each other in the developing cross-linking network. In this case, we observe morphological transitions from the initial domain morphology with a large-curvature interface to another domain morphology with a smaller-curvature interface, such as the transition from the cylindrical phase to the lamellar phase. We calculated the spatial correlations in the microphase-separated domains and found that such correlations are affected by the speed of the formation of the cross-linking network depending on whether the bridging between microphase-separated domains occurs in a nucleation and growth process or in a spinodal decomposition process.

Quantification of natural rubber blends by reflection/reflectance infrared and confocal Raman spectroscopy: a comparison of statistical methods.

The blend of butadiene and acrylonitrile copolymer (NBR) with natural poly-cis-isoprene (NR) shows increased resistance to swelling in solvents in comparison to the individual components. In aerospace, NBR rubber is used as thermal protection for rockets and shall not contain other polymers, even in low contents, otherwise, it can affect the protection performance and rocket safety by causing detachment of the elastomer/propellant interface; therefore, this investigation presents methodologies to determine the NR/NBR contents. This study explores different analytical techniques, such as Raman spectroscopy and Fourier transform infrared (FTIR) spectroscopy, in the mid-infrared (MIR) by reflection and in the near-infrared by reflectance (NIRA) modes, Furthermore, quantification strategies by univariate, bivariate and multivariate (chemometric) models are evaluated and compared. A proposed methodology, based on multivariate Raman microscopy with partial least squares regression (PLS), showed high linearity (R2 > 0.99) and low error (< 0.82 %). The validation of FT-MIR data for the CH3, which presented lower error (1.3%) than vinylidene band (6%), showed that both methodologies (reflection and NIRA reflectance) can be used for the quantification of NR in NR/NBR. These results constitute a contribution to the state of the art in researching industrial and aerospace elastomeric applications.

Nanostructures and toughening mechanisms in lightly cross-linked all-methacrylate copolymer/functional block copolymer blends

Nanostructures and toughening mechanisms in lightly cross-linked all-methacrylate copolymer/functional block copolymer blends

Enhancing the transparency and tensile properties of immiscible poly(methyl methacrylate)/ethylene-vinyl alcohol copolymer blends by lithium salt addition

Enhancing the transparency and tensile properties of immiscible poly(methyl methacrylate)/ethylene-vinyl alcohol copolymer blends by lithium salt addition

Investigation of Crystallization, Morphology, and Mechanical Properties of Polypropylene/Polypropylene-Polyethylene Block Copolymer Blends.

Polyethylene (PE)-based elastomers are the ideal choice for enhancing the compatibility of polypropylene/polyethylene (PP/PE) blends and improving the mechanical properties of PP-based materials. However, the issue of blend systems lies in the interplay between the crystallization processes. Therefore, we investigated the crystallization behavior during the cooling process of a new generation of PP/PE block copolymers (PP-b-PE) and random polypropylene (PPR, a copolymer of propylene and a small amount of ethylene or an alpha-olefin) blends using in-situ X-ray diffraction/scattering and differential scanning calorimetry (DSC) techniques. We also conducted mechanical performance tests on PPR/PP-b-PE blends at room temperature and low temperature (-5 °C). The results indicate that during the cooling process, the PP phase of PP-b-PE will follow the PPR to crystallize in advance and form a eutectic mixture, thereby enhancing the compatibility of PP/PE. Moreover, the PPR/PP-b-PE blend will form stable β-(300) crystals with excellent mechanical properties. Due to the improved compatibility of PP/PE with PP-b-PE, PE crystals are dispersed within PP crystals, providing bonding that improves the toughness of PPR under the low stiffness failure conditions of PPR/PP-b-PE blends, thereby enhancing their impact performance at low and room temperatures. This research has great significance for both recycling waste plastics and enhancing the low-temperature toughness of PPR.

Optimization and analysis of Sic reinforced copolymer blend composite structural springs

The design of lightweight leaf springs plays a crucial role in reducing fuel consumption and improving vehicle comfort by minimizing road shock transmission and vibration. Composite materials have shown great potential in significantly reducing leaf spring weight. epoxy, being a desirable thermoset polymer widely used in various applications such as electrical devices, ships and automobiles, exhibits limitations in terms of brittleness, fracture resistance and impact strength. To overcome these drawbacks while preserving its beneficial properties, epoxy can be blended with other polymers and reinforcements. In this study, polysulfide (PS) was selected as a suitable solution to enhance epoxy brittleness, offering an effective yet underutilized approach. Furthermore, the incorporation of silicon carbide (Sic), known for its superior characteristics, aimed to further enhance the mechanical properties of the epoxy-PS copolymer blend. The microstructural analysis was inspected using Fourier transform infrared. The blending and reinforcement process followed a Taguchi L8 static design to evaluate the impact of different composite blending percentages (represented as input factors) on leaf spring tensile strength, damping properties, impact resistance and hardness (represented as responses). The responses were analyzed using S/N ratios, ANOVA, main effect plots and interaction plots, while regression equations were employed to predict the responses under varying factors. The analysis demonstrated a robust model for manufacturing leaf springs. Experimental results indicated a 7.4% reduction in hardness with the addition of PS polymer. Conversely, reinforcing the epoxy-PS copolymer with 10–20% wt. of Sic resulted in a 3–5% increase in hardness. The natural frequency of the composite exhibited a gradual decrease upon the incorporation of PS and Sic. Evaluating the damping ratio revealed that the maximum value was achieved when the epoxy-PS copolymer was reinforced with 20% Sic. Additionally, while the copolymer blend displayed the greatest logarithmic decrement, epoxy exhibited the highest damping frequency.

Morphologies, structures, and properties on blends of triblock copolymers and linear low-density polyethylene

Abstract Focusing on the study of the phase separation behavior of triblock copolymer and linear low-density polyethylene (LLDPE) systems helps to understand the influence of microstructure on the properties of poly(vinylcyclohexane)-b- poly(ethylene)-b-poly(vinylcyclohexane) (PVCH-PE-PVCH/LLDPE) blends. We prepared a series of blends of LLDPE and PVCH-PE-PVCH and explained their compatibility from the microstructure. The research findings indicate that despite having similar block compositions, PVCH-PE-PVCH with a higher molecular weight exhibits significantly stronger phase separation and crystallization ability compared to PVCH-PE-PVCH with lower molecular weight. In PVCH-PE-PVCH/LLDPE blends, the addition of 10 %, 20 %, and 30 % LLDPE induces earlier crystallization and crystal phase separation of polyethylene (PE) fragments. In addition, compared to the lower molecular weight of PVCH-PE-PVCH, the higher molecular weight of PVCH-PE-PVCH exhibits a higher tendency for independent crystallization and shows significant crystal phase separation during the cooling crystallization process when blended with LLDPE. The PE segments in the lower molecular weight of PVCH-PE-PVCH can more easily enter the nanoscale domain of LLDPE. Impact fracture electron microscopy also reveals better compatibility between the lower molecular weight of PVCH-PE-PVCH and LLDPE compared to the higher molecular weight of PVCH-PE-PVCH. Furthermore, the blends of lower molecular weight of PVCH-PE-PVCH and LLDPE exhibit a greater growth rate in elongation at break.

In Vitro and In Vivo Hydrolytic Degradation Behaviors of a Drug-Delivery System Based on the Blend of PEG and PLA Copolymers.

This paper presents the in vitro and in vivo degradation of BEPO, a marketed in situ forming depot technology used for the formulation of long-acting injectables. BEPO is composed of a solution of a blend of poly(ethylene glycol)-block-poly(lactic acid) (PEG-PLA) triblock and diblock in an organic solvent, where a therapeutic agent may be dissolved or suspended. Upon contact with an aqueous environment, the solvent diffuses and the polymers precipitate, entrapping the drug and forming a reservoir. Two representative BEPO compositions were subjected to a 3-month degradation study in vitro by immersion in phosphate-buffered saline at 37 °C and in vivo after subcutaneous injection in minipig. The material erosion rate, as a surrogate of the bioresorption, determined via the depot weight loss, changed substantially, depending on the composition and content of polymers within the test item. The swelling properties and internal morphology of depots were shown to be highly dependent on the solvent exchange rate during the precipitation step. Thermal analyses displayed an increase of the depot glass transition temperature over the degradation process, with no crystallinity observed at any stage. The chemical composition of degraded depots was determined by 1H NMR and gel permeation chromatography and demonstrated an enrichment in homopolymers, i.e., free PLA and (m)PEG, to the detriment of (m)PEG-PLA copolymers in both formulations. It was observed that the relative ratio of the degradants within the depot is driven by the initial polymer composition. Interestingly, in vitro and in vivo results showed very good qualitative consistency. Taken together, the outcomes from this study demonstrate that the different hydrolytic degradation behaviors of the BEPO compositions can be tuned by adjusting the polymer composition of the formulation.

Understanding the Seeded Heteroepitaxial Growth of Crystallizable Polymers: The Role of Crystallization Thermodynamics.

Seeded heteroepitaxial growth is a "living" crystallization-driven self-assembly (CDSA) method that has emerged as a promising route to create uniform segmented nanoparticles with diverse core chemistries by using chemically distinct core-forming polymers. Our previous results have demonstrated that crystallization kinetics is a key factor that determines the occurrence of heteroepitaxial growth, but an in-depth understanding of controlling heteroepitaxy from the perspective of crystallization thermodynamics is yet unknown. Herein, we select crystallizable aliphatic polycarbonates (PxCs) with a different number of methylene groups (xCH2, x = 4, 6, 7, 12) in their repeating units as model polymers to explore the effect of lattice match and core compatibility on the seeded growth behavior. Seeded growth of PxCs-containing homopolymer/block copolymer blend unimers from poly(ε-caprolactone) (PCL) core-forming seed platelet micelles exhibits distinct crystal growth behavior at subambient temperatures, which is governed by the lattice match and core compatibility. A case of seeded growth with better core compatibility and a smaller lattice mismatch follows epitaxial growth, where the newly created crystal domain has the same structural orientation as the original platelet substrate. In contrast, a case of seeded growth with better core compatibility but a larger lattice mismatch shows nonepitaxial growth with less-defined crystal orientations in the platelet plane. Additionally, a case of seeded growth with poor core compatibility and larger lattice mismatch results in polydisperse platelet micelles, whereby crystal formation is not nucleated from the crystalline substrate. These findings reveal important factors that govern the specific crystal growth during a seeded growth approach by using compositionally distinct cores, which would further guide researchers in designing 2D segmented materials via polymer crystallization approaches.

Influence of the Main Blown Film Extrusion Process Parameters on the Mechanical Properties of a High-Density Polyethylene Hexene Copolymer and Linear Low-Density Polyethylene Butene Copolymer Blend Used for Plastic Bags

Polyethylene plastic bags manufactured via blown film extrusion have different quality specifications depending on their intended use. It is known that the mechanical properties of a film depend on the process parameters established, but little is known concerning how they affect one another, even more so due to the variety of polyethylene materials and processing techniques. This study focuses on establishing a proper correspondence of important mechanical properties like the dart impact, tensile strength at break, and elongation at break with commonly used process parameters like the blow-up ratio, take-up ratio, thickness reduction, and neck height, for a high-density polyethylene hexene copolymer and a linear low-density polyethylene butene copolymer blend film. Because this polyethylene mixture is an anisotropic material, interesting R2 values equal to or higher than 0.90 were found: a BUR with elongation at break and tensile strength at break in the MD and TD, a TUR with elongation at break in the MD and tensile strength at break in the MD and TD, and a TR with elongation at break and tensile strength at break in the MD. Also, a relationship between the dart impact and both the neck height and thickness were found.

Design of Copolymer‐Based Blend Compatibilizers for Mixed Plastic Recycling

AbstractMixed plastic waste recycling represents a significant challenge as the phase separation of different components dictates downgraded performance. Polymer‐based compatibilizers can offer a promising solution to address this issue, through effectively reducing surface tension and increasing interfacial strength between distinct components to result in improved mechanical and thermal properties of recycled products. This perspective provides an overview of the fundamental concepts for the rational design of copolymer blend compatibilizers and discusses their recent advances, including both preformed and in situ generated systems. Impacts of key material parameters of compatibilizers, such as chain topology, chemical composition, and block sequence on their performance of remediating mixed plastics are discussed. Additionally, reactive compatibilization strategies are also introduced, including in situ formation of polymers, installing functional groups on mixed plastics, and employing dual compatibilization strategies. Looking forward, there are many research and technology opportunities in this area, especially for enabling the use of blend compatibilizers to practically address mixed plastic wastes at scale. Specifically, future compatibilizer design and application should provide strong competitiveness in both cost and energy savings, and carbon emission reduction. Together, the development of blend compatibilizers is an important step in establishing plastic circular economy and creating a more sustainable future.

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.