Mechanical Properties Of Polymers Research Articles

Generation of Microplastics from Biodegradable Packaging Films Based on PLA, PBS and Their Blend in Freshwater and Seawater.

Biodegradable polymers and their blends have been advised as an eco-sustainable solution; however, the generation of microplastics (MPs) from their degradation in aquatic environments is still not fully grasped. In this study, we investigated the formation of bio-microplastics (BMPs) and the changes in the physicochemical properties of blown packaging films based on polylactic acid (PLA), polybutylene succinate (PBS) and a PBS/PLA 70/30 wt% blend after degradation in different aquatic media. The tests were carried out in two temperature/light conditions to simulate degradation in either warm water, under sunlight exposure (named Warm and Light-W&L), and cold deep water (named Cold and Dark-C&D). The pH changes in the aqueous environments were evaluated, while the formed BMPs were analyzed for their size and shape alongside with variations in polymer crystallinity, surface and mechanical properties. In W&L conditions, for all the films, the hydrolytic degradation led to the reorganization of the polymer crystalline phases, strong embrittlement and an increase in hydrophilicity. The PBS/PLA 70/30 blend exhibited increased resistance to degradation with respect to the neat PLA and PBS films. In C&D conditions, no microparticles were observed up to 12 weeks of degradation.

Advancing Structural Supercapacitors with Hydrated Polymer

Structural supercapacitors, capable of bearing mechanical loads while storing electrical energy, hold great promise for enhancing mobile system efficiencies. However, developing practical structural supercapacitors often involves a challenging balance between mechanical and electrochemical performance, particularly in their electrolytes. Traditional research has focused on bi-continuous phase electrolytes (BPEs), which typically comprise high liquid content that weakens mechanical strength, and inert solid phases that hinder ion conduction and block electrode surfaces. Our previous work introduces a novel approach with a hydrated polymer electrolyte, demonstrating enhanced multifunctionality. This electrolyte, derived from controlled hydration of PET-LiClO4, forms a trihydrate (LiClO4∙3H2O) structure, where water molecules bond with ions without forming a liquid phase, thereby improving ion mobility while maintaining the base polymer's mechanical properties. This new design also promotes better electrochemical interfaces with electrodes, a significant advancement over traditional BPEs.In this study, we further enhance the performance and processability of such hydrated polymer electrolytes by incorporating polylactic acid (PLA) as the base polymer and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) as the salt. The electrolyte, prepared through solution casting and subsequent controlled hydration, consistently remains an amorphous solid solution in both dry and hydrated states, as confirmed by DSC, XRD, and FTIR analyses. Our tests on ionic conductivity and mechanical properties reveal that adding water to the polymer electrolyte substantially increases ionic conductivity while retaining mechanical properties. A specific composition demonstrated a remarkable increase in ionic conductivity coupled with superior toughness surpassing the base polymer. Furthermore, we successfully fabricated and tested structural supercapacitor devices made of composites of carbon fibers and these new electrolytes. The prototypes presented enhanced toughness with significant energy storage performance, demonstrating their vast application potential due to their outstanding multifunctionality.

Metamaterial design for aortic aneurysm simulation using 3D printing

IntroductionThe use of three-dimensional (3D) printed anatomic models is steadily increasing in research and as a tool for clinical decision-making. The mechanical properties of polymers and metamaterials were investigated to evaluate their application in mimicking the biomechanics of the aortic vessel wall.MethodologyUniaxial tensile tests were performed to determine the elastic modulus, mechanical stress, and strain of 3D printed samples. We used a combination of materials, designed to mimic biological tissues’ properties, the rigid VeroTM family, and the flexible Agilus30™. Metamaterials were designed by tessellating unit cells that were used as lattice-reinforcement to tune their mechanical properties. The lattice-reinforcements were based on two groups of patterns, mainly responding to the movement between links/threads (chain and knitted) or to deformation (origami and diamond crystal). The mechanical properties of the printed materials were compared with the characteristics of healthy and aneurysmal aortas.ResultsUniaxial tensile tests showed that the use of a lattice-reinforcement increased rigidity and may increase the maximum stress generated. The pattern and material of the lattice-reinforcement may increase or reduce the strain at maximum stress, which is also affected by the base material used. Printed samples showed max stress ranging from 0.39 ± 0.01 MPa to 0.88 ± 0.02 MPa, and strain at max stress ranging from 70.44 ± 0.86% to 158.21 ± 8.99%. An example of an application was created by inserting a metamaterial designed as a lattice-reinforcement on a model of the aorta to simulate an abdominal aortic aneurysm.ConclusionThe maximum stresses obtained with the printed models were similar to those of aortic tissue reported in the literature, despite the fact that the models did not perfectly reproduce the biological tissue behavior.

Thermomechanical properties of multifunctional polymer hybrid nanocomposites based on carbon nanotubes and nanosilica

AbstractNanocomposites containing low wt% of oxidized multi‐walled carbon nanotubes (MWCNT‐OXI), nanosilica (NS), and its hybrid (MWCNT‐OXI/NS) in epoxy resin were produced and evaluated. The used nanoparticles were studied by scanning electron microscopy (SEM), thermogravimetric analysis (TGA), and Raman spectroscopy while the nanocomposites were investigated in relation to its morphology, thermal, and mechanical properties. The results demonstrated significant improvements in the storage modulus (E′), glass transition temperature (Tg), and cross link density (CD), for the produced nanocomposites. Increases in thermal conductivity (TC) of up to 85% at 90°C were observed for the nanocomposites containing 1.0 wt% of the hybrid MWCNT‐OXI + NS nanofiller, when compared with neat polymer. It was also verified increases in the resistance to plastic deformation for the nanocomposites, maintained the polymer thermal stability with the addition of these nanoparticles. Finally, the use of MWCNT‐OXI and NS, combined or not, significantly improved the thermal and mechanical properties of polymer, showing multifunctional characteristics for the produced nanocomposites.

Entanglements of Macromolecules and Their Influence on Rheological and Mechanical Properties of Polymers.

Flexible macromolecules easily become entangled with neighboring macromolecules. The resulting network determines many polymer properties, including rheological and mechanical properties. Therefore, a number of experimental and modeling studies were performed to describe the relationship between the degree of entanglement of macromolecules and polymer properties. The introduction presents general information about the entanglements of macromolecule chains, collected on the basis of studies of equilibrium entangled polymers. It is also shown how the density of entanglements can be reduced. The second chapter presents experiments and models leading to the description of the movement of a single macromolecule. The next part of the text discusses how the rheological properties change after partial disentangling of the polymer. The results on the influence of the degree of chain entanglement on mechanical properties are presented.

Mechanical Properties of Polymer Reinforced Concrete at High Strain Rate and Analysis of Its Micro-mechanism

Mechanical Properties of Polymer Reinforced Concrete at High Strain Rate and Analysis of Its Micro-mechanism

Photoinduced Reversible Disentanglement-Entanglement Transition in partially miscible azobenzene polymer blends

Entanglements, an intrinsic feature of long chains, are critical to the rheological and mechanical properties of polymers. Adding low molecular weight solvents or oligomers into entangled polymers can reduce the entanglements, but the entanglement cannot recover without removing the solvents. Reversible control of the entanglement degree is still a big challenge. In this work, we introduce the azobenzene polymer (Pazo) with reversible photoswitchable side-chain conformation as dynamic diluent into entangled poly(butyl methacrylate) (PBMA) to form a partially miscible blend system. The reduction of entanglement of PBMA by trans-Pazo is similar to a typical solvent, while an unexpectedly stronger tube dilation effect was found for cis-Pazo. Cis-Pazo/PBMA blends exhibit a stronger dependence of plateau modulus on PBMA content, GN(φ)∼φ4.5, which is significantly different from the well-established relation GN(φ)∼φ2 for polymer solutions and blends. The cis-Pazo can disentangle PBMA at a much lower concentration (∼55 %) than the trans-Pazo (>70 %). Pazo content of 55 %–70 % can induce a completely unentangled state of PBMA in Pazo/PBMA blends when Pazo is in the cis state after UV light irradiation, and the entanglement can recover when it is transformed to the trans state. Adding azobenzene polymer does not alter the activation energy of the re-entanglement process.

How Depolymerization-Based Plasticization Affects the Process of Cold Crystallization in Poly(P-Dioxanone).

The self-plasticization, i.e., the increase in the polymer chains' mobility by including its monomer, has a major impact on a polymer's structural, thermal, and mechanical properties. In this study, differential scanning calorimetry (DSC), optical and Raman microscopies, thermo-mechanical analysis (TMA), size exclusion chromatography equipped with a multi-angle light scattering detector (SEC-MALS), and X-ray diffraction analysis (XRD) are used to investigate the effect of thermally induced self-plasticization of poly-(p-dioxanone), PDX, on the crystal growths from the amorphous and molten states. Significant changes in the crystallization behavior and mechanical properties of PDX are found only for samples self-plasticized at the depolymerization temperature (Td) above 150°C. The intense self-plasticization leads to the decrease of the crystallization temperature, increase of the crystal growth rapidity, disappearance of the distinct α→α' polymorphic transition, reduction of the overall melting temperature, and segregation of the redundant monomer. Although the morphology of the crystalline phase has a major impact on the mechanical properties of PDX, the self-plasticization itself does not seem to result in any major changes in the magnitude, localization, or morphology of formed crystallites (these are primarily driven by the temperature of crystal growth). The manifestation of the variable activation energy concept is discussed for the present crystallization data.

Analysis of fracture damage mechanical properties of particle reinforced polymer composite film based on micro-macro finite element method

The particle reinforcement and related effect on fracture damage mechanical properties of polymers have been studied in this paper. Based on the uniaxial tensile test result of SiO2 particle reinforced polyvinylidene fluoride (PVDF) composites, the parameters of macro elastic-plastic finite element model and micro particle reinforced model are obtained. The effects of boundary conditions, shape and size of damage notch on fracture damage mechanical properties of PVDF composites are studied from macroscopic view. The uniaxial tensile mechanical properties and elastic modulus are increased with notch angle (0°, 30°, 60°, 120°). The damage analysis of the micro model shows that the mechanical properties of SiO2/PVDF composites are best when the content of SiO2 is 6%. Debonding between particles and matrix indicates have great effect on crack propagation. The micro-macro finite element model is effective tool to study the damage mechanical properties of particle reinforced polymers.

Using the Quartz Crystal Microbalance to Monitor the Curing of Drying Oils.

Drying oils such as linseed oil form a polymer network through a complex free-radical polymerization process. We have studied polymerization in this challenging class of polymers using a quartz crystal microbalance (QCM). The QCM is able to measure the evolution of polymer mass and mechanical properties as the oil transitions from a liquid-like to a solid-like state. Measurements using bulk materials and thin films provide information about the initial polymerization phase as well as the evolution of the mass and mechanical properties over the first two years of cure. The temperature-dependent response of the cured linseed oil films was also measured. These results were combined with previously published results obtained from traditional dynamic mechanical analysis to give a unified picture of the properties of these materials across a very broad temperature range.

Effect of cage and ladder configuration of polyphenyl silsesquioxane on mechanical performance and flame retardancy of ethylene–vinyl acetate composites

Improving the flame retardancy of ethylene–vinyl acetate copolymer (EVA) while maintaining its mechanical properties is critical for EVA applications. Polyhedral oligomeric silsesquioxane (POSS) can be a molecular structure designed to improve the flame retardancy of polymers while minimizing damage to the mechanical properties of polymers. In this study, two types of POSS with the same chemical structure but different spatial structures, which are named cage octaphenyl POSS (OPS) and ladder polyphenyl silsesquioxane (PPSQ) are prepared. The miscibility and dispersibility of these two types of POSS in the EVA matrix and their effects on mechanical properties, dielectric properties, and fire behaviors are also investigated. Compared to OPS-based EVA composite, the PPSQ with ladder structure has good miscibility and dispersion state in EVA matrix, obtaining better toughness, dielectric properties, and flame retardancy under cone calorimeter test. However, OPS-based EVA composite obtains superior flame retardancy than that of PPSQ-based EVA composite under small fire test (limiting oxygen index and UL-94 vertical burning tests). The mechanism of these two separate flame-retardant performances under various scenarios is explored. A novel flame-retardant model is proposed, as well as a new understanding of the role of POSS in EVA combustion. This study provides powerful guidance for obtaining EVA composites with excellent flame retardant and mechanical properties.

Friction stir spot welding of recycled scrap thermoplastics

There is a real demand for sustainable lightweight structures because of the growing environmental concerns. One important solution is developing structures through recycled scrap/waste thermoplastic materials. The current work studies the friction stir spot weldability of recycled thermoplastics, which will help to analyze the potential of friction stir-based welding techniques towards developing these sustainable structures. The combined behavior of recycling-welding procedures is investigated, as they may cause degradations; to ensure that the base thermoplastic polymer's chemical, thermal, and mechanical properties are retained. Scrapped milk bottles made from HDPE material are used as a case study. The highest lap-shear load of 1528 N was achieved at the optimum welding conditions of 1600 rpm rotational speed, 1 mm plunge depth, and 60 s dwell time. Fractographic studies (macroscopic and SEM-based) suggested four types of fracture morphologies depending on welding conditions used. The DSC results showed no significant differences in melting temperature and crystalline content of the polymeric material. The TGA tests showed no significant thermal degradations. The FTIR analysis of all the samples (bottle, recycled sheet, weld material) exhibited characteristic HDPE peaks. All these results suggest combined-welding recycling had a minimal impact on the polymeric structure. Thus, friction stir spot welding (FSSW) technique joins recycled thermoplastic scrap/waste materials with high lap-shear load and without any significant polymer degradations.

Combined effect of montmorillonite Cloisite 30B and graphene nanoplatelets on high‐density polyethylene matrix under high strain rate dynamic compression

AbstractLaminated polymer composites are widely used in ballistic barriers where polyethylene can be applied. The mechanical properties of polymers can be improved with the addition of nanofillers. Therefore, this work evaluates the effect of the combination of montmorillonite Cloisite 30B (OMt) and graphene (Gr) on the dynamics compression properties obtained from a split‐Hopkinson pressure bar (SHPB) test for nanostructured maleinized high‐density polyethylene (HDPE). The nanofillers are incorporated into the polymeric matrix in its molten state, and their dispersion is evaluated through x‐ray diffraction and transmission electron microscopy analyses. Thermal analysis, including differential scanning calorimetry and thermogravimetric analysis are performed. Additionally, the viscoelastic behavior of the materials is studied from the results of storage and loss modulus obtained by dynamic‐mechanical analysis. Under the SHPB test conditions, it is possible to evaluate the material stress–strain curve, identifying its yield point, compressive strength, and deformations to calculate the elastic stiffness and toughness of the material. The nanocomposite with 3% OMt and 0.75% Gr (wt.%) shows the highest average compressive strength and toughness values. Furthermore, this sample shows similar Tpeak temperature, improved crystallinity index, storage, and loss modulus, with similar glass transition temperature compared to the HDPE sample.

Modulus alteration of thin polystyrene films by their neighboring PDMS: Soft and hard confinement.

It is highly demanded to understand the confinement effect on nanoconfined polymers. Recent studies reported a strong perturbation of local dynamics and substantial alteration of glass transition temperature Tg at nanoscale. However, how confinement affects the mechanical properties of polymers is not fully understood. Here, we show that the modulus of thin polymer films could be remarkedly altered through a polymer-polymer interface. The modulus of a thin polystyrene (PS) film next to a polydimethylsiloxane (PDMS) was determined from the PS-PDMS bilayer bulging test. A series of experiments show that the modulus of PS can be increased up to 37%, when the modulus of the neighboring PDMS varies from 1.04 to 4.88 MPa. The results demonstrate a strong sensitivity of mechanical properties of thin polymers to the hard/soft environment, which we attribute to the change of high-mobility layer by the polymer-polymer interface.

Research of the influence of temperature on the physical and mechanical properties of polymers for the manufacture of LED lamp housings

Methods for predicting of the influence of temperature on the physical and mechanical properties of structural polymer composite materials under development used in LED lamps are considered. Using the differential scanning calorimetry, the specific heat capacity and phase transformations of light-conducting polymers and samples of housings for lamps being developed are studied. The choice of fillers is carried out taking into account the optimization of the composition of polymer materials. Keywords:research, polymeric materials, temperature, hardness, elastic modulus, specific heat capacity, thermal analysis alekc_sap@mail.ru

Drug-Modified Contact Lenses-Properties, Release Kinetics, and Stability of Active Substances with Particular Emphasis on Cyclosporine A: A Review.

The following review focuses on the manufacturing and parameterizing of ocular drug delivery systems (DDS) using polymeric materials to create soft contact lenses. It discusses the types of drugs embedded into contact lenses, the various polymeric materials used in their production, methods for assessing the mechanical properties of polymers, and techniques for studying drug release kinetics. The article also explores strategies for investigating the stability of active substances released from contact lenses. It specifically emphasizes the production of soft contact lenses modified with Cyclosporine A (CyA) for the topical treatment of specific ocular conditions. The review pays attention to methods for monitoring the stability of Cyclosporine A within the discussed DDS, as well as investigating the influence of polymer matrix type on the stability and release of CyA.

Regulation of the Properties of Polymers based on Thiirane using Mixtures of Amine Hardeners

Abstract: Introduction: The possibility of regulating the curing rate and the complex of adhesive, deformation-strength and dynamic mechanical properties of polymers based on bisphenol A dithioester (thiirane) using a mixture of amine hardeners of various chemical nature is investigated. Method: Diethylenetriamine, diethylenetriaminomethylphenol and aminopolyamide were investigated as hardeners. The ratio of the components of the mixed hardener is selected, which provides the best combination of strength properties. Results: It was found that the rate of adhesion and cohesive strength at the initial stage (during the first hour) of curing compositions containing a mixture hardener significantly exceeds compositions cured by individual components of the mixture. Conclusion: The results of measuring the dynamic mechanical characteristics of the studied polymers indicate that the dynamic modulus of elasticity, measured at temperatures below and above the transition from a glassy state to a high elastic one, for a sample containing a mixed hardener has an intermediate value between the values characteristic of samples containing individual components of a mixed hardener. objective: The ratio of the components of the mixed hardener is selected, which provides the best combination of strength properties.

Mechanical properties of polymer modified mortars using polymer latexes with varied glass transition temperature and surface charges

Mechanical properties of polymer modified mortar (PMM) were investigated using self-synthesized polymer latexes with varied glass transition temperature (Tg) and colloidal surface charges to build correlations between the mechanical properties of PMMs and the intrinsic properties of the polymers. Generally, compressive strength and elastic modulus of mortar are decreased, but ductility and toughness are enhanced by incorporation of the polymers. Impacts of the lower Tg polymers on the mechanical properties of PMMs are more pronounced. With increasing polymer content, flexural and tensile strength of mortar first increase and then decrease when using low Tg polymers that form continuous film during hardening of the mortars, while steadily decrease in the case of high Tg polymers that exist as individual particles in the hardened PMMs. For the high Tg polymer modified mortars, it is interestingly found that a subsequential heat treatment effectively promotes the film formation of the polymers in the hardened PMMs and thus greatly increases their flexural and tensile strength. This indicates that polymer film formation is essential to the enhancement of the PMMs, because the polymer films play a crack-bridging effect while the individual particles cannot do such job. The high Tg polymers lead to higher tensile strength of PMMs after heat treatment due to the higher inherent strength of the polymer film. Higher colloidal surface charge benefits the mechanical properties of the PMMs by (1) promoting a more homogenous polymer distribution in the hardened PMMs and/or (2) improving the bonding between the polymer phase and cement hydrates.

Effects of blending poly (polyol sebacate) and poly (polyol adipate) bioelastomers for soft tissue engineering in biomedical applications

AbstractIn this article, the synthesis of four novel bioelastomers known as poly (xylitol sebacate) (PXS), poly (xylitol adipate) (PXA), poly (sorbitol sebacate) (PSS), and poly (sorbitol adipate) (PSA) was carried out through bulk polymerization, followed by their blending using the solution method. Six blends were prepared namely PXS25/PSS75, PXS50/PSS50, PXS75/PSS25, PXS50/PXA50, PSA50/PXA50, and PSS50/PSA50. After blending, a thermal curing process was applied to the samples. The intrinsic viscosity, density, Tg, hydrophilicity, degradation, wound healing, and mechanical properties of polymers and blends were measured to investigate the effects of blending. Analyzing hardness, modulus, stress at breakpoint, degradation, and hydrophilicity data showed that the mechanical properties of bioelastomers are adjustable by blending for tissue engineering. Furthermore, the scratch assay proved the biocompatibility of pure polymers and indicated that blending does not have a negative impact on this matter.

Highly thermally conductive composites with boron nitride nanoribbon array

The traditional approaches to fabricate highly thermally conductive yet electrically insulating polymers relies mainly on adding massive ceramic fillers, which not only degrade the mechanical properties of polymers but also introduce more interfaces that lead to more scattering sites for phonons. Thus, it remains a major challenge to achieve high thermal conductivity with low filler content. Herein, to create directional conductors with fewer interfaces, we prepared array of vertically aligned hexagonal boron nitride nanoribbons (BNNRs) and then infused them with polydimethylsiloxane (PDMS). By optimizing the assembly density and crystalline structure of the BNNRs, the BNNR/PDMS composite achieves a remarkable through-plane thermal conductivity of 8.19 W/(m·K) at a low nanoribbon loading of 9.3 wt%, outperforming thermally conductive polymers with insulating fillers in spherical, fibrous, and flaky shapes at similar filler contents. Furthermore, high thermal–mechanical stability and outstanding electrical insulating properties are also discovered. In the thermal interface material (TIM) performance test, the BNNR/PDMS composite exhibits higher cooling efficiency than commercial TIMs, with a decrease in chip temperature of up to 16 °C, and maintains good thermal stability even after continuous heating–cooling processes of as long as 12 h.