Mechanical Properties Of Polymers Research Articles

Visible-light-switchable glass transition temperatures and optical actuation in crosslinked fluoroazopolymers

Nature has provided significant inspiration for designing polymer materials that can move in response to light, with many examples of such materials created, especially using ultraviolet (UV) light as an external stimulus. However, it is essential to design materials that can regulate the mechanical properties of polymers through visible light stimulation and macroscale movement under visible light exposure. Here, we have developed a polymer film chemically crosslinked with fluorinated azobenzenes, which produces a strong mechanical response when exposed to green or blue light in air. The film exhibits visible-light-switchable mechanical properties and directional bending due to the photoisomerization of azo chromophores in the crosslinked polymer networks. The thin film also changes their optical transparency upon visible light irradiation. This work offers insights into the development of responsive polymer materials and photomechanical materials, advancing the realization of self-propelled machines and soft robotics powered by visible light.

Investigation of the Effect of Reprocessing on Thermal and Mechanical Properties of Polymers and Polymer Nanocomposites

This study explored the impact of multiple reprocessing cycles on the thermomechanical properties of polystyrene (PS) and low‐density polyethylene (LDPE), simulated through reprocessing with a twin‐screw extruder. Additionally, it compared the thermal and mechanical properties of graphene nanoplatelets (1% w/w) reinforced polypropylene (PP‐GNP) nanocomposites with PP. The materials undergo seven consecutive extrusion cycles at varying screw speeds (100 and 150 rpm) and temperatures (180 and 200 °C). Increasing the screw speed from 100 to 150 rpm raised LDPE's screw torque by about 40% at the first reprocessing cycle. Processing PS at 200 °C reduced screw torque by ≈20% compared to 180 °C at 1–5 reprocessing cycles. Both torque and power decrease for PP and PP‐GNP with each reprocessing cycle. LDPE's tensile modulus decreases with more cycles at 200 °C, while PS shows no consistent variation. PP's tensile modulus and ultimate tensile strength drop by 24% and 12%, respectively, from the first to the fifth cycle, while PP‐GNP exhibits no consistent variation. Differential scanning calorimetry shows no clear change in LDPE's melting point, but an increase in PP and PP‐GNP's melting points up to the fifth cycle. This research provides crucial insights to advance the recycling of polymers reducing environmental impact.

Tailoring Wetting Ridge Dynamics on Hybrid Acrylic Polymers: The Impact of Mechanical Properties on Continuous Wetting.

This study examined the relationships among the wetting speed, the polymer mechanical properties, and the resulting deformation characteristics of various graft copolymers synthesized from acrylic monomers and acrylated l-lactide and ε-caprolactone macromonomers (MMs). The mechanical properties of the polymer films were manipulated with minimal impact on their static contact angles with water by varying their MM composition. The focus was on wetting speeds prior to the onset of stick-slip behavior, where ridges were smoothly pulled over the surfaces, thereby producing a transient deformation indicative of a wave pulse. The height of the propagated ridge structures quickly converged to a steady-state value, depending on the wetting speed and polymer properties, regardless of the initial size. The results show that the propagated ridge height correlates with the wetting speed, and the data are well fitted by the Kelvin-Voigt model, which yields two key parameters: the maximum ridge height at the limit of zero velocity and the characteristic wetting speed. Both parameters correlated linearly with the lactide content in the MMs, and the characteristic wetting speed correlated linearly with crossover frequencies from the rheological master curves of the polymers. Furthermore, the characteristic wetting speed was correlated with the peel force required to remove polymer films from the steel plates, establishing a connection between dynamic wetting and adhesive behavior. Our findings shed light on the interdependence between the material composition, mechanical properties, and wetting behavior. The insights presented offer significant potential for designing materials with controlled wetting properties, particularly for applications where capillary flow and surface interactions play critical roles.

Investigation of the mechanical properties of polymer based on Tetra Pak waste

Investigation of the mechanical properties of polymer based on Tetra Pak waste

Machine learning can predict the mechanical properties of polymers

Machine learning can predict the mechanical properties of polymers

Ease-of-manufacture highly transparent thin polyvinyl alcohol aerogel

The earliest silicon-based aerogels attracted attention due to their nanoscale porous structure and high transparency. Still, they need to be more balanced with the poor mechanical properties. Their brittle structure limits the development of this promising new material. Therefore, the goal of this work is to optimize the mechanical properties of aerogels while maintaining transparency. The good mechanical properties of polymers have made them the material of choice for this work. Polyvinyl alcohol (PVA), which can undergo self-crosslinking through side-chain hydroxyl groups forming hydrogen bonds, was chosen as the raw material to simplify and expedite the production process. The production process was experimented with, analyzed, and refined. Considering the time efficiency of the experimental process, a one-step gelling method was invented to facilitate the sol-gel transition. The one-step gelling method maintained the high transparency of PVA aerogels and reduced the time required for the gelation process compared to the freeze-thawing method. This work employs carbon dioxide supercritical drying to ensure minimal structural collapse and maximize the porous structure’s retention. The transmittance of PVA aerogels can reach up to 93.67% at a wavelength of 1333 nm. The internal structure of aerogels with different PVA concentrations was observed using a Scanning electron microscope. Applying Beer-Lambert’s Law eliminated the effect of sample thickness on transparency. The relationship between the transparency of PVA aerogels, their microstructure, and macroscopic concentration was studied and analyzed for the first time. While ensuring light transmittance, the modulus of the PVA aerogel reached as high as 6.18 ± 0.56 MPa at 13 wt%.

Advanced functional polymer materials for biomedical applications

AbstractPolymer structures are essential in biomedical applications due to their biocompatibility, biodegradability, and ability to form intricate structures on micro‐ to nanometer scales. This review, emphasizing electrospinning and phase inversion techniques, examines the fabrication strategies and chemical design of polymer structures for biomedical use. Electrospinning, particularly needleless electrospinning, produces nanofibres with high porosity and flexibility and is widely applied in tissue engineering and drug delivery. Phase inversion, including thermal, nonsolvent‐, vapor‐ and evaporation‐induced phase separation, allows precise control over polymer properties but faces challenges in terms of cooling rates and solvent characteristics. Chemical design through doping, functionalization, cross‐linking and copolymerization enhances the biocompatibility, biodegradability and mechanical properties of polymers, facilitating advanced applications in drug delivery, tissue scaffolding and biosensors. Advanced functional polymers are revolutionizing biomedical fields, offering innovative solutions for therapeutic medicine delivery, disease detection, diagnostics, and regenerative medicine. Despite remarkable progress, challenges, such as scalability, cost‐effectiveness, and environmental impact, persist. This review underscores the transformative potential of advanced polymer materials in medical treatments and advocates for continuous research and interdisciplinary collaboration to overcome existing challenges and fully exploit the capabilities of these materials in improving patient care and medical outcomes. Future perspectives highlight enhancing precision control mechanisms, integrating phase inversion with other techniques and developing large‐scale production methods to advance the field further.

Effects of the Blend Ratio and Operating Conditions (T and P) on the Thermal and Mechanical Properties of Polymer (EVA-113/Nitrile-Butadiene Rubber) Blends Prepared by Supercritical CO2

Effects of the Blend Ratio and Operating Conditions (<i>T</i> and <i>P</i>) on the Thermal and Mechanical Properties of Polymer (EVA-113/Nitrile-Butadiene Rubber) Blends Prepared by Supercritical CO₂

Systematic screening of particle engineered polymers for the preparation of multiparticulates embedded orally disintegrating tablets

This paper evaluated polymers' physical and mechanical properties to formulate modified-release multiparticulates to be embedded in orally disintegrating tablets (ODTs). The targeted polymer should have adequate elastic-plastic properties in a multiparticulate system during the manufacturing process, which is affected by its physical properties. The good mechanical properties of the multiparticulate system can effectively aid in retaining the shape of the particles from being affected under applied compression pressure during the formulation process and tablets preparations. Therefore, the formulation should have good mechanical attains. Five polymers (three natural and two synthetic), namely: sodium alginate, polyvinyl alcohol (PVA), methylcellulose (MC), polyacrylic acid (PAA) and Eudragit L100, were evaluated. Polymers in raw form or particle engineered using spray drying were characterised using different analysis techniques: differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), compacts tensile strength, texture analysis, particle size analysis and surface area analysis. The unprocessed PAA exhibited the lowest Young's modulus, measuring at 5.38 MPa, whereas MC displayed the highest value of 14.74 MPa. The polymers were subjected to spray drying at a concentration of 5% w/v. Data of the texture analysis revealed that Young's modulus increased for the spray-dried PAA powder, reaching 13.69 MPa. This suggests an enhanced polymer compressibility subsequent to the spray drying process. Eudragit L100 demonstrated an enhanced tabletability prolife after spray drying. SEM and surface area results showed a correlation with the mechanical findings. Plasticity and elasticity together provide strong, durable tablets with structural integrity. Achieving a balance between these properties is crucial for effective tabletability. The results of this study provide an insight into physical and mechanical properties and changes encountered upon spray drying. A balance between elastic- plastic properties is required for optimal multiparticulate development.

A theoretical approach based on machine learning for estimation of physical properties of LLDPE in moulding process

This study explores the prediction of mechanical characteristics of linear polyethylene based on oven residence time, employing various regression models and hyper-parameter tuning through the Whale Optimization Algorithm. The dataset comprises one input variable (oven residence time) and three output parameters (Tensile Strength, Impact Strength, and Flexure Strength). The models investigated include Multilayer Perceptron, K-Nearest Neighbors, Support Vector Regression, Polynomial Regression, and Theil–Sen Regression. The results showcased distinct performances across the models for each output parameter. The Polynomial Regression (WOA-PR) method has been identified as the most suitable option for predicting Tensile Strength due to its ability to achieve the lowest errors in terms of Mean Absolute Error, Root Mean Square Error, and Average Absolute Relative Deviation. K-Nearest Neighbors (WOA-KNN) outperforms other models in predicting Impact Strength due to its superior accuracy and reliability. Additionally, Support Vector Regression (WOA-SVR) emerges as the best model for predicting Flexure Strength, showcasing notable performance in minimizing prediction errors. These findings underscore the significance of model selection and optimization techniques in accurately predicting the mechanical properties of polymers, paving the way for enhanced manufacturing processes and material design.

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.

Designing of carbon nanohorn‐based heterostructure for improved mechanical properties, flame retardancy, and hydrophobicity of composite aerogels

AbstractDeveloping flame‐resistant thermal insulation aerogels with strong mechanical properties is crucial for addressing the fire hazards in high‐rise buildings. Carbon nanomaterials have garnered significant attention for enhancing the flame retardancy and mechanical properties of polymers due to their safety, nontoxicity, and low additions. In this work, the effect of single‐walled carbon nanohorns (SWCNHs) on the mechanical properties, thermal insulation properties, thermal stability, flame retardancy, and hydrophobicity of polyvinyl alcohol/KH560/phytic acid composite aerogel (PKASx) was investigated. By adjusting the concentration of SWCNHs, the mechanical properties of the aerogel were significantly improved, owing to robust interactions between SWCNHs and the matrix. However, a declining trend was observed in both the compressive modulus and specific modulus when the quantity of SWCNHs exceeded 0.3%. Simultaneously, the PKAS0.3 aerogel exhibited remarkable flame retardancy and self‐extinguishing characteristics. It possessed a high LOI value of 34.2 ± 0.2%, with a 25.2% reduction in pHRR and an 18.6% reduction in THR. Moreover, the analysis of TSP and SPR curves affirmed that the inclusion of SWCNHs effectively minimized the production of gaseous by‐products during combustion. In addition, the introduction of SWCNHs introduced a trade‐off in the roughness of the aerogel. The maximum contact angle occurred at the optimal concentration of SWCNHs.

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.