Polymers

24 pages, 5584 KiB

Open AccessReview

A Review on Polymers for Biomedical Applications on Hard and Soft Tissues and Prosthetic Limbs

by Heitor Luiz Ornaghi, Jr., Francisco Maciel Monticeli and Lucas Dall Agnol

Polymers 2023, 15(19), 4034; https://doi.org/10.3390/polym15194034 - 9 Oct 2023

Cited by 9 | Viewed by 3320

In the past decades, there has been a significant increase in the use of polymers for biomedical applications. The global medical polymer market size was valued at USD 19.92 billion in 2022 and is expected to grow at a CAGR of 8.0% from [...] Read more.

In the past decades, there has been a significant increase in the use of polymers for biomedical applications. The global medical polymer market size was valued at USD 19.92 billion in 2022 and is expected to grow at a CAGR of 8.0% from 2023 to 2030 despite some limitations, such as cost (financial limitation), strength compared to metal plates for bone fracture, design optimization and incorporation of reinforcement. Recently, this increase has been more pronounced due to important advances in synthesis and modification techniques for the design of novel biomaterials and their behavior in vitro and in vivo. Also, modern medicine allows the use of less invasive surgeries and faster surgical sutures. Besides their use in the human body, polymer biomedical materials must have desired physical, chemical, biological, biomechanical, and degradation properties. This review summarizes the use of polymers for biomedical applications, mainly focusing on hard and soft tissues, prosthetic limbs, dental applications, and bone fracture repair. The main properties, gaps, and trends are discussed. Full article

(This article belongs to the Special Issue Advanced Polymer Hybrid Materials)

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11 pages, 2107 KiB

Open AccessArticle

Acoustofluidics-Assisted Coating of Microparticles

by Ming-Lin Yeh, Geng-Ming Chang and Yi-Je Juang

Polymers 2023, 15(19), 4033; https://doi.org/10.3390/polym15194033 - 9 Oct 2023

Cited by 1 | Viewed by 1605

Abstract

Microparticles have been applied in many areas, ranging from drug delivery, diagnostics, cosmetics, personal care, and the food industry to chemical and catalytic reactions, sensing, and environmental remediation. Coating further provides additional functionality to the microparticles, such as controlled release, surface modification, bio-fouling [...] Read more.

Microparticles have been applied in many areas, ranging from drug delivery, diagnostics, cosmetics, personal care, and the food industry to chemical and catalytic reactions, sensing, and environmental remediation. Coating further provides additional functionality to the microparticles, such as controlled release, surface modification, bio-fouling resistance, stability, protection, etc. In this study, the conformal coating of microparticles with a positively charged polyelectrolyte (polyallylamine hydrochloride, PAH) by utilizing an acoustofluidic microchip was proposed and demonstrated. The multiple laminar streams, including the PAH solution, were formed inside the microchannel, and, under the traveling surface acoustic wave, the microparticles traversed through the streams, where they were coated with PAH. The results showed that the coating of microparticles can be achieved in a rapid fashion via a microfluidic approach compared to that obtained by the batch method. Moreover, the zeta potentials of the microparticles coated via the microfluidic approach were more uniform. For the unfunctionalized microparticles, the charge reversal occurred after coating, and the zeta potential increased as the width of the microchannel or the concentration of the PAH solution increased. As for the carboxylate-conjugated microparticles, the charge reversal again occurred after coating; however, the magnitudes of the zeta potentials were similar when using the microchannels with different widths or different concentrations of PAH solution. Full article

(This article belongs to the Topic Micro/Nanofluidics and Structures Based Sensing, Material Processing and Energy Conversion)

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27 pages, 3782 KiB

Open AccessReview

A Review of Solid-State Proton–Polymer Batteries: Materials and Characterizations

by M. S. A. Rani, M. N. F. Norrrahim, V. F. Knight, N. M. Nurazzi, K. Abdan and S. H. Lee

Polymers 2023, 15(19), 4032; https://doi.org/10.3390/polym15194032 - 9 Oct 2023

Viewed by 1901

Abstract

The ever-increasing global population necessitates a secure and ample energy supply, the majority of which is derived from fossil fuels. However, due to the immense energy demand, the exponential depletion of these non-renewable energy sources is both unavoidable and inevitable in the approaching [...] Read more.

The ever-increasing global population necessitates a secure and ample energy supply, the majority of which is derived from fossil fuels. However, due to the immense energy demand, the exponential depletion of these non-renewable energy sources is both unavoidable and inevitable in the approaching century. Therefore, exploring the use of polymer electrolytes as alternatives in proton-conducting batteries opens an intriguing research field, as demonstrated by the growing number of publications on the subject. Significant progress has been made in the production of new and more complex polymer-electrolyte materials. Specific characterizations are necessary to optimize these novel materials. This paper provides a detailed overview of these characterizations, as well as recent advancements in characterization methods for proton-conducting polymer electrolytes in solid-state batteries. Each characterization is evaluated based on its objectives, experimental design, a summary of significant results, and a few noteworthy case studies. Finally, we discuss future characterizations and advances. Full article

(This article belongs to the Special Issue Advances in Polymer Applied in Batteries and Capacitors)

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15 pages, 5165 KiB

Open AccessArticle

Effect of Rice Husk and Wood Flour on the Structural, Mechanical, and Fire-Retardant Characteristics of Recycled High-Density Polyethylene

by Atta Ur Rehman Shah, Abdul Jalil, Atiya Sadiq, Meshal Alzaid, Muhammad Shoaib Naseem, Rakan Alanazi, Sultan Alanazi, Abdullatyf Obaid Alanzy, Ibrahim Hotan Alsohaimi and Rizwan Ahmed Malik

Polymers 2023, 15(19), 4031; https://doi.org/10.3390/polym15194031 - 9 Oct 2023

Cited by 4 | Viewed by 2000

Abstract

Given the rising consumption of plastic products, it is becoming imperative to prioritize the recycling of plastic items as a solution to reducing plastic waste and environmental pollution. In this context, this research focuses on assessing the impact of incorporating rice husk and [...] Read more.

Given the rising consumption of plastic products, it is becoming imperative to prioritize the recycling of plastic items as a solution to reducing plastic waste and environmental pollution. In this context, this research focuses on assessing the impact of incorporating rice husk and wood flour into recycled high-density polyethylene (rec-HDPE) to analyze its mechanical properties, flammability, and thermal stability. The combined rec-HDPE content of wood flour and rice husk varied between 0% and 20%. The rec-HDPE content of maleic anhydride grafted polyethylene (MAPE) was fixed at 3%. Mechanical characteristics such as flexural, tensile, and impact strengths were assessed. Cone calorimetry (CC) tests, limited oxygen index (LOI) tests, and horizontal and vertical burning tests were performed to determine the flammability or fire retardancy of these composites. On the other hand, to characterize the thermal characteristics of these composites, thermogravimetric analysis (TGA) was used. To further characterize the fluctuation in these characteristics, scanning electron microscopy (SEM) and infrared spectroscopy (FTIR) studies were carried out. The mechanical characteristics were found to be increased in response to adding rice husk or wood flour. An 8% increase in tensile strength and a 20% increase in elastic modulus enhancement were recorded for a 20% rice husk-added composite. SEM revealed the reason for the variation in tensile properties, based on the extent of agglomeration and the extent of uniform distribution of fillers in rec-HDPE. Following these lines, the 20% rice husk-added composite also showed a maximum increase of around 6% in its flexural strength and a maximum increase of 50% in its flexural modulus. A decrease in impact strength was recorded for rice husk and wood flour-reinforced composites, compared with unreinforced rec-HDPE. Hybrid composites displayed a lack of mechanical strength due to changes in their nature. FTIR tests were performed for a much more elaborate analysis to confirm these results. Twenty percent of rice husk-added rec-HDPE displayed the best thermal properties that were tested, based on TGA and derivative thermogravimetric (DTG) analysis. This 20% composite also displayed the best fire-retardancy characteristics according to UL 94 tests, cone calorimetry tests, and limited oxygen index tests, due to the barrier created by the silica protective layer. These tests demonstrated that the incorporation of both fillers—rice husk and wood flour—effectively enhanced the thermal, mechanical, and fire-retardant attributes of recycled HDPE. Full article

(This article belongs to the Special Issue Computational and Experimental Approaches in Polymeric Materials)

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16 pages, 2912 KiB

Open AccessArticle

Investigation of Novel Flax Fiber/Epoxy Composites with Increased Biobased Content

by Bianca Dal Pont, Vito Gigante, Luca Panariello, Ilaria Canesi, Laura Aliotta and Andrea Lazzeri

Polymers 2023, 15(19), 4030; https://doi.org/10.3390/polym15194030 - 9 Oct 2023

Cited by 3 | Viewed by 1853

Abstract

Currently, biobased epoxy resins derived from plant oils and natural fibers are available on the market and are a promising substitute for fossil-based products. The purpose of this work is to investigate novel lightweight thermoset fiber-reinforced composites with extremely high biobased content. Paying [...] Read more.

Currently, biobased epoxy resins derived from plant oils and natural fibers are available on the market and are a promising substitute for fossil-based products. The purpose of this work is to investigate novel lightweight thermoset fiber-reinforced composites with extremely high biobased content. Paying attention to the biobased content, following a cascade pathway, many trials were carried out with different types of resins and hardeners to select the best ones. The most promising formulations were then used to produce flax fiber reinforced composites by vacuum bagging process. The main biocomposite properties such as tensile, bending, and impact properties as well as the individuation of their glass transition temperatures (by DSC) were assessed. Three biocomposite systems were investigated with biobased content ranging from 60 to 91%, obtaining an elastic modulus that varied from 2.7 to 6.3 GPa, a flexural strength from 23 to 108.5 MPa, and Charpy impact strength from 11.9 to 12.2 kJ/m². The properties reached by the new biocomposites are very encouraging; in fact, their stiffness vs. lightweight (calculated by the E/ρ³ ratio) is comparable to some typical epoxy–glass composites. Full article

(This article belongs to the Special Issue Biobased and Biodegradable Polymer Blends and Composites II)

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30 pages, 6101 KiB

Open AccessReview

From Nature to Technology: Exploring Bioinspired Polymer Actuators via Electrospinning

by Muhammad Yasar Razzaq, Maria Balk, Magdalena Mazurek-Budzyńska and Anke Schadewald

Polymers 2023, 15(19), 4029; https://doi.org/10.3390/polym15194029 - 9 Oct 2023

Cited by 3 | Viewed by 2036

Abstract

Nature has always been a source of inspiration for the development of novel materials and devices. In particular, polymer actuators that mimic the movements and functions of natural organisms have been of great interest due to their potential applications in various fields, such [...] Read more.

Nature has always been a source of inspiration for the development of novel materials and devices. In particular, polymer actuators that mimic the movements and functions of natural organisms have been of great interest due to their potential applications in various fields, such as biomedical engineering, soft robotics, and energy harvesting. During recent years, the development and actuation performance of electrospun fibrous meshes with the advantages of high permeability, surface area, and easy functional modification, has received extensive attention from researchers. This review covers the recent progress in the state-of-the-art electrospun actuators based on commonly used polymers such as stimuli-sensitive hydrogels, shape-memory polymers (SMPs), and electroactive polymers. The design strategies inspired by nature such as hierarchical systems, layered structures, and responsive interfaces to enhance the performance and functionality of these actuators, including the role of biomimicry to create devices that mimic the behavior of natural organisms, are discussed. Finally, the challenges and future directions in the field, with a focus on the development of more efficient and versatile electrospun polymer actuators which can be used in a wide range of applications, are addressed. The insights gained from this review can contribute to the development of advanced and multifunctional actuators with improved performance and expanded application possibilities. Full article

(This article belongs to the Special Issue Shape-Memory Polymers for Multiple Applications in the Materials World)

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14 pages, 3219 KiB

Open AccessArticle

Evidence through Thermal Analysis of Retro Diels-Alder Reaction in Model Networks Based on Anthracene Modified Polyester Resins

by Daniela Ionita, Mariana Cristea, Constantin Gaina, Mihaela Silion and Bogdan C. Simionescu

Polymers 2023, 15(19), 4028; https://doi.org/10.3390/polym15194028 - 9 Oct 2023

Viewed by 1380

Abstract

The present work is focused on polyester resins obtained from the diglycidyl ether of bisphenol A and anthracene modified 5-maleimidoisophthalic acid. Because the maleimide-anthracene Diels–Alder (DA) adduct is stable at high temperatures, it is considered a good option for high performance polymers. However, [...] Read more.

The present work is focused on polyester resins obtained from the diglycidyl ether of bisphenol A and anthracene modified 5-maleimidoisophthalic acid. Because the maleimide-anthracene Diels–Alder (DA) adduct is stable at high temperatures, it is considered a good option for high performance polymers. However, the information related to the retroDA reaction for this type of adduct is sometimes incoherent. A detailed thermal study (conventional TGA, HiRes TGA, MTGA, DSC, MDSC) was performed in order to establish whether the rDA reaction can be revealed for this type of anthracene modified polyester resins. The TGA method confirmed the cleavage of the anthracene–maleimide DA adduct, while the DSC demonstrated the presence of anthracene in the system. At high temperatures, unprotected maleimide homopolymerizes and/or reacts with allyl groups according to the –ene reaction. Therefore, the thermal DA reaction is not displayed anymore upon the subsequent cooling, and the glass transition region is registered at a higher temperature range during the second heating. The use of sample-controlled thermal analysis (HiRes TGA) and MTGA improved the TGA result; however, it was not possible to separate the very complex degradation processes that are interconnected. Full article

(This article belongs to the Special Issue Self-Healing Polymers, Proteins and Composites)

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25 pages, 14676 KiB

Open AccessArticle

Experimental and Analytical Studies on Low-Cost Glass-Fiber-Reinforced-Polymer-Composite-Strengthened Reinforced Concrete Beams: A Comparison with Carbon/Sisal Fiber-Reinforced Polymers

by Kittipoom Rodsin, Ali Ejaz, Qudeer Hussain and Rattapoohm Parichatprecha

Polymers 2023, 15(19), 4027; https://doi.org/10.3390/polym15194027 - 9 Oct 2023

Cited by 5 | Viewed by 1356

Abstract

This study presents an experimental framework with seventeen beams to investigate the impact of loading type, configuration, and through-bolt anchorage on LC-GFRP (Low-Cost Glass-Fiber-Reinforced Polymer) confinement performance. Beams underwent three-point and four-point bending, with LC-GFRP applied in various ways, including U-shaped, side-bonded, and [...] Read more.

This study presents an experimental framework with seventeen beams to investigate the impact of loading type, configuration, and through-bolt anchorage on LC-GFRP (Low-Cost Glass-Fiber-Reinforced Polymer) confinement performance. Beams underwent three-point and four-point bending, with LC-GFRP applied in various ways, including U-shaped, side-bonded, and fully wrapped, with and without anchors. The performance of LC-GFRP was compared to CFRP (Carbon-Fiber-Reinforced Polymer) and sisal wraps. LC-GFRP in side-bonded and U-shaped configurations without anchors under three-point bending showed no shear failure, while those under four-point bending without anchors experienced shear failure. With anchors, U-shaped configurations successfully prevented shear failure. The side-bonded, U-shaped, and U-shaped configurations along the full span with anchors demonstrated peak capacity enhancements of 72.11%, 43.66%, and 68.39% higher improvements than the corresponding configurations without anchors, respectively. Wrapping all sides of the beam with LC-GFRP or CFRP prevented shear failure without additional anchors, with complete wrapping being the most efficient method. When anchors were used, significant capacity enhancements were observed. Existing shear strength prediction models were evaluated, highlighting the need for more tailored expressions for LC-GFRP confinement, especially for non-U-shaped configurations. Full article

(This article belongs to the Section Polymer Applications)

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23 pages, 14518 KiB

Open AccessArticle

Self-Lubricating and Shape-Stable Phase-Change Materials Based on Epoxy Resin and Vegetable Oils

by Svetlana O. Ilyina, Irina Y. Gorbunova, Veronika V. Makarova, Michael L. Kerber and Sergey O. Ilyin

Polymers 2023, 15(19), 4026; https://doi.org/10.3390/polym15194026 - 9 Oct 2023

Viewed by 1454

Abstract

Palm or coconut oil is capable of dissolving in a mixture of bisphenol A-based epoxy resin and a high-temperature hardener (4,4′-diaminodiphenyl sulfone) when heated and then forms a dispersed phase as a result of cross-linking and molecular weight growth of the epoxy medium. [...] Read more.

Palm or coconut oil is capable of dissolving in a mixture of bisphenol A-based epoxy resin and a high-temperature hardener (4,4′-diaminodiphenyl sulfone) when heated and then forms a dispersed phase as a result of cross-linking and molecular weight growth of the epoxy medium. Achieving the temporary miscibility between the curing epoxy matrix and the vegetable oil allows a uniform distribution of vegetable oil droplets in the epoxy medium. This novel approach to creating a dispersed phase-change material made a cured epoxy polymer containing up to 20% oil. The miscibility of epoxy resin and oil was studied by laser interferometry, and phase state diagrams of binary mixtures were calculated according to theory and experiments. A weak effect of oil on the viscosity and kinetics of the epoxy resin curing was demonstrated by rotational rheometry. According to differential scanning calorimetry and dynamic mechanical analysis, the oil plasticizes the epoxy matrix slightly, expanding its glass transition region towards low temperatures and reducing its elastic modulus. In the cured epoxy matrix, oil droplets have a diameter of 3–14 µm and are incapable of complete crystallization due to their multi-component chemical composition and non-disappeared limited miscibility. The obtained phase-change materials have relatively low specific energy capacity but can be used alternatively as self-lubricating low-noise materials due to dispersed oil, high stiffness, and reduced friction coefficient. Palm oil crystallizes more readily, better matching the creation of phase-change materials, whereas coconut oil crystallization is more suppressed, making it better for reducing the friction coefficient of the oil-containing material. Full article

(This article belongs to the Special Issue Polymeric Phase Change Materials)

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11 pages, 2724 KiB

Open AccessArticle

Tough and Robust Metallosupramolecular Hydrogels Enabled by Ti₃C₂T_x MXene Nanosheets

by Biqiang Jin, Wenqiang Wu, Zhaoyang Yuan and Changcheng Wang

Polymers 2023, 15(19), 4025; https://doi.org/10.3390/polym15194025 - 9 Oct 2023

Cited by 1 | Viewed by 1094

Abstract

Recently, many tough synthetic hydrogels have been created as promising candidates in fields such as smart electronic devices. In this paper, we propose a simple strategy to construct tough and robust hydrogels. Two-dimensional Ti₃C₂T_x MXene nanosheets and metal [...] Read more.

Recently, many tough synthetic hydrogels have been created as promising candidates in fields such as smart electronic devices. In this paper, we propose a simple strategy to construct tough and robust hydrogels. Two-dimensional Ti₃C₂T_x MXene nanosheets and metal ions were introduced into poly(acrylamide-co-acrylic acid) hydrogels, the MXene nanosheets acted as multifunctional cross-linkers and effective stress-transfer centers, and physical cross-links were formed between Fe³⁺ and carboxylic acid. Under deformation, the coordination interactions exhibit reversible dissociation and reorganization properties, suggesting a novel mechanism of energy dissipation and stress redistribution. The design enabled the hydrogel to exhibit outstanding and balanced mechanical properties (tensile strength of up to 5.67 MPa and elongation at break of up to 508%). This study will facilitate the diverse applications of metallosupramolecular hydrogels. Full article

(This article belongs to the Special Issue Recent Advances in Applied Soft Matter)

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12 pages, 8770 KiB

Open AccessArticle

Supramolecular Responsive Chitosan Microcarriers for Cell Detachment Triggered by Adamantane

by Lixia Huang, Yifei Jiang, Xinying Chen, Wenqi Zhang, Qiuchen Luo, Siyan Chen, Shuhan Wang, Fangqing Weng and Lin Xiao

Polymers 2023, 15(19), 4024; https://doi.org/10.3390/polym15194024 - 8 Oct 2023

Viewed by 1359

Abstract

Supramolecular responsive microcarriers based on chitosan microspheres were prepared and applied for nonenzymatic cell detachment. Briefly, chitosan microspheres (CSMs) were first prepared by an emulsion crosslinking approach, the surface of which was then modified with β-cyclodextrin (β-CD) by chemical grafting. Subsequently, gelatin was [...] Read more.

Supramolecular responsive microcarriers based on chitosan microspheres were prepared and applied for nonenzymatic cell detachment. Briefly, chitosan microspheres (CSMs) were first prepared by an emulsion crosslinking approach, the surface of which was then modified with β-cyclodextrin (β-CD) by chemical grafting. Subsequently, gelatin was attached onto the surface of the CSMs via the host–guest interaction between β-CD groups and aromatic residues in gelatin. The resultant microspheres were denoted CSM-g-CD-Gel. Due to their superior biocompatibility and gelatin niches, CSM-g-CD-Gel microspheres can be used as effective microcarriers for cell attachment and expansion. L-02, a human fetal hepatocyte line, was used to evaluate cell attachment and expansion with these microcarriers. After incubation for 48 h, the cells attached and expanded to cover the entire surface of microcarriers. Moreover, with the addition of adamantane (AD), cells can be detached from the microcarriers together with gelatin because of the competitive binding between β-CD and AD. Overall, these supramolecular responsive microcarriers could effectively support cell expansion and achieve nonenzymatic cell detachment and may be potentially reusable with a new cycle of gelatin attachment and detachment. Full article

(This article belongs to the Special Issue Research Progress on Chitosan Applications)

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13 pages, 9595 KiB

Open AccessArticle

Effects of Modifying Agent and Conductive Hybrid Filler on Butyl Rubber Properties: Mechanical, Thermo-Mechanical, Dynamical and Re-Crosslinking Properties

by Piyawedee Luangchuang, Tanawat Sornanankul and Yeampon Nakaramontri

Polymers 2023, 15(19), 4023; https://doi.org/10.3390/polym15194023 - 8 Oct 2023

Viewed by 1435

Abstract

Ionic crosslinking of bromobutyl rubber (BIIR) composites was prepared using butylimidazole (IM) and ionic liquid (IL), combined with carbon nanotubes (CNT) and conductive carbon black (CCB) to enhance the intrinsic properties and heal ability of the resulting composites. Variation in the BIIR/CNT-CCB/IM/IL ratios [...] Read more.

Ionic crosslinking of bromobutyl rubber (BIIR) composites was prepared using butylimidazole (IM) and ionic liquid (IL), combined with carbon nanotubes (CNT) and conductive carbon black (CCB) to enhance the intrinsic properties and heal ability of the resulting composites. Variation in the BIIR/CNT-CCB/IM/IL ratios was investigated to determine the appropriate formulation for healing the composites. Results showed that the mechanical properties were increased until the IM:IL:CNT/CCB ratio reached 1:1:1/1.5, corresponding to the optimal concentration of 5:5:5/7.5 phr. Thermo-oxidative degradation, as indicated using temperature scanning stress relaxation (TSSR), demonstrated the decomposition of the composites at higher temperatures, highlighting the superior resistance provided by the proper formulation of BIIR composites. Additionally, the conditions for the healing procedure were examined by applying pressure, temperature, and time. It was observed that the composites exhibited good elasticity at 0 °C and 60 °C, with a high rate of re-crosslinking achieved under appropriate pressure and temperature conditions. This research aims to develop a formulation suitable for the tire tread and inner liner of commercial car tires together with artificial skin products. Full article

(This article belongs to the Special Issue Cross-Linked Polymers II)

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15 pages, 4620 KiB

Open AccessArticle

Examining the Quasi-Static Uniaxial Compressive Behaviour of Commercial High-Performance Epoxy Matrices

by J. F. Gargiuli, G. Quino, R. Board, J. C. Griffith, M. S. P. Shaffer, R. S. Trask and I. Hamerton

Polymers 2023, 15(19), 4022; https://doi.org/10.3390/polym15194022 - 8 Oct 2023

Cited by 1 | Viewed by 1548

Abstract

Four commercial high-performance aerospace aromatic epoxy matrices, CYCOM^®890, CYCOM^®977-2, PR520, and PRISM EP2400, were cured to a standardised 2 h, 180 °C cure cycle and evaluated in quasi-static uniaxial compression, as well as by dynamic scanning calorimetry (DSC) and [...] Read more.

Four commercial high-performance aerospace aromatic epoxy matrices, CYCOM^®890, CYCOM^®977-2, PR520, and PRISM EP2400, were cured to a standardised 2 h, 180 °C cure cycle and evaluated in quasi-static uniaxial compression, as well as by dynamic scanning calorimetry (DSC) and thermogravimetric analysis (TGA). The thermoplastic toughened CYCOM^®977-2 formulation displayed an overall increase in true axial stress values across the entire stress–strain curve relative to the baseline CYCOM^®890 sample. The particle-toughened PR520 sample exhibited an overall decrease in true axial stress values past the yield point of the material. The PRISM EP2400 resin, with combined toughening agents, led to true axial stress values across the entire plastic region of the stress–strain curve, which were in line with the stress values observed with the CYCOM^®890 material. Interestingly, for all formulations, the dilation angles (associated with the volume change during plastic deformation), recorded at 0.3 plastic strain, were close to 0°, with the variations reflecting the polymer structure. Compression data collected for this series of commercial epoxy resins are in broad agreement with a selection of model epoxy resins based on di- and tetra-functional monomers, cured with polyamines or dicarboxylic anhydrides. However, the fully formulated resins demonstrate a significantly higher compressive modulus than the model resins, albeit at the expense of yield stress. Full article

(This article belongs to the Special Issue Mechanics of Polymeric Structures across Scales)

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10 pages, 220 KiB

Open AccessEditorial

Eco Polymeric Materials and Natural Polymer

by Jingpeng Li, Yun Lu and Huiqing Wang

Polymers 2023, 15(19), 4021; https://doi.org/10.3390/polym15194021 - 8 Oct 2023

Cited by 4 | Viewed by 2736

Abstract

With the increasing concern regarding the undesirable environmental and socioeconomic consequences of petrochemicals and limited fossil resources, biomass, bio-based polymers, and other renewable natural resources have increasingly become alternatives for the production of functional materials [...] Full article

(This article belongs to the Special Issue Eco Polymeric Materials and Natural Polymer)

11 pages, 3367 KiB

Open AccessArticle

Mechanical Robust, Self-Healable Polyurethane Elastomer Enabled by Hierarchical Hydrogen Bonds and Disulfide Bonds

by Biqiang Jin, Wenqiang Wu and Haitao Wu

Polymers 2023, 15(19), 4020; https://doi.org/10.3390/polym15194020 - 8 Oct 2023

Cited by 4 | Viewed by 1913

Abstract

The fabrication of mechanically robust and self-healing polymeric materials remains a formidable challenge. To address the drawbacks, a core strategy is proposed based on the dynamic hard domains formed by hierarchical hydrogen bonds and disulfide bonds. The dynamic hard domains dissipate considerable stress [...] Read more.

The fabrication of mechanically robust and self-healing polymeric materials remains a formidable challenge. To address the drawbacks, a core strategy is proposed based on the dynamic hard domains formed by hierarchical hydrogen bonds and disulfide bonds. The dynamic hard domains dissipate considerable stress energy during stretching. Meanwhile, the synergistic effect of hierarchical hydrogen bonds and disulfide bonds greatly enhances the relaxation dynamics of the PU network chains, thus accelerating network reorganization. Therefore, this designed strategy effectively solves the inherent drawback between cohesive energy and relaxation dynamics of the PU network. As a result, the PU elastomer has excellent mechanical properties (9.9 MPa and 44.87 MJ/m³) and high self-healing efficiency (96.2%). This approach provides a universal but valid strategy to fabricate high-performance self-healing polymeric materials. Meanwhile, such materials can be extended to emerging fields such as flexible robotics and wearable electronics. Full article

(This article belongs to the Special Issue Recent Advances in Applied Soft Matter)

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18 pages, 3176 KiB

Open AccessArticle

Investigation of the Gas Permeation Properties Using the Volumetric Analysis Technique for Polyethylene Materials Enriched with Pure Gases under High Pressure: H₂, He, N₂, O₂ and Ar

by Ji-Hun Lee, Ye-Won Kim and Jae-Kap Jung

Polymers 2023, 15(19), 4019; https://doi.org/10.3390/polym15194019 - 7 Oct 2023

Cited by 3 | Viewed by 1588

Abstract

Polyethylene (PE) is widely used as a gas-sealing material in packing films and gas transport pipes. A technique for evaluating the permeability of water-insoluble gases has recently been developed. This technique is a volumetric analysis that is used to calculate the gas permeability [...] Read more.

Polyethylene (PE) is widely used as a gas-sealing material in packing films and gas transport pipes. A technique for evaluating the permeability of water-insoluble gases has recently been developed. This technique is a volumetric analysis that is used to calculate the gas permeability by measuring the gas uptake and diffusivity. With this technique, we investigated the permeability of pure gases, such as H₂, He, N₂, O₂ and Ar, enriched under high pressure up to 9 MPa in low-density polyethylene (LDPE), ultrahigh molecular weight polyethylene (UHMWPE) and high-density polyethylene (HDPE). The gas uptake showed a linear pressure-dependent behavior that followed Henry’s law, and the diffusivity was independent of the pressure. Furthermore, the logarithmic diffusivity values of the five gases linearly decreased as their molecular kinetic diameters increased. The logarithmic solubility values linearly increased as the critical temperatures of the gases increased. The calculated permeability results were correlated with the volume fraction of the amorphous phase and the fractional free volume. This result newly showed that the amorphous phase was directly correlated to the fractional free volume. Full article

(This article belongs to the Section Polymer Analysis and Characterization)

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12 pages, 2645 KiB

Open AccessArticle

Density Fluctuations Inside an Individual Polymer Coil

by Anatoly E. Chalykh, Uliana V. Nikulova, Vladimir K. Gerasimov and Vladimir V. Matveev

Polymers 2023, 15(19), 4018; https://doi.org/10.3390/polym15194018 - 7 Oct 2023

Viewed by 922

Abstract

More than five hundred images of individual macromolecules of random styrene-butadiene copolymers and styrene-isoprene block copolymers dissolved in a polystyrene matrix were analyzed. The presence of density fluctuations inside the macromolecular coil has been established. Within the framework of the model of harmonic [...] Read more.

More than five hundred images of individual macromolecules of random styrene-butadiene copolymers and styrene-isoprene block copolymers dissolved in a polystyrene matrix were analyzed. The presence of density fluctuations inside the macromolecular coil has been established. Within the framework of the model of harmonic oscillations, the radial distribution of such density fluctuations is estimated. Full article

(This article belongs to the Special Issue Polymer Dynamics: From Single Chains to Networks and Gels)

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23 pages, 9040 KiB

Open AccessArticle

Degradation of Structurally Modified Polylactide under the Controlled Composting of Food Waste

by Elena Trofimchuk, Valeria Ostrikova, Olga Ivanova, Marina Moskvina, Anna Plutalova, Tatyana Grokhovskaya, Anna Shchelushkina, Alexander Efimov, Elena Chernikova, Shenghua Zhang and Vladimir Mironov

Polymers 2023, 15(19), 4017; https://doi.org/10.3390/polym15194017 - 7 Oct 2023

Cited by 3 | Viewed by 2039

Abstract

The degradation of polylactide (PLA) films of different structures under conditions of controlled composting has been studied. We have demonstrated that PLA underwent degradation within one month in a substrate that simulated standard industrial composting. Regardless of the initial structure of the samples, [...] Read more.

The degradation of polylactide (PLA) films of different structures under conditions of controlled composting has been studied. We have demonstrated that PLA underwent degradation within one month in a substrate that simulated standard industrial composting. Regardless of the initial structure of the samples, the number-average molecular weight (M_n) decreased to 4 kDa while the degree of crystallinity increased to about 70% after 21 days of composting. Addition of an inoculant to the standard substrate resulted in the accelerated degradation of the PLA samples for one week due to an abiotic hydrolysis. These findings have confirmed that industrial composting could solve the problem of plastic disposal at least for PLA. Full article

(This article belongs to the Special Issue Natural and Industrial Waste Based Polymer Composites: Processing, Characterization and Applications)

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16 pages, 10049 KiB

Open AccessArticle

Oxy-Butane Ablation Testing of Thermal Protection Systems Based on Nanomodified Phenolic Resin Matrix Materials

by George Pelin, Cristina Elisabeta Pelin, Adriana Stefan, Violeta Tsakiris, Alexandra Ana Maria Panait and Emil Costea

Polymers 2023, 15(19), 4016; https://doi.org/10.3390/polym15194016 - 7 Oct 2023

Viewed by 1392

Abstract

Two classes of thermal protection systems composed of a carbon-fibre-reinforced (CFRP) layer and an ablative material layer joined with a thermo-resistant ceramic adhesive were developed. The two classes differ in the composition of the ablative material reinforcing compound. In the first class, the [...] Read more.

Two classes of thermal protection systems composed of a carbon-fibre-reinforced (CFRP) layer and an ablative material layer joined with a thermo-resistant ceramic adhesive were developed. The two classes differ in the composition of the ablative material reinforcing compound. In the first class, the ablative material is based on micronic-sized cork granules, and in the second class, the ablative material is reinforced with carbonic felt. For both classes of thermal protection systems, the reinforcement material was impregnated in simple phenolic resin, and nanometric additive, consisting of silicon carbide nanoparticles added in two different weight contents (1 and 2% by weight) relative to the resin. The thermal conductivity for the ablative materials in the thermal protection systems structure was determined. A test facility using oxy-butane flame was developed through which the thermal protection systems developed were tested at extreme temperatures, to simulate some thermal conditions in space applications. The materials were characterised from a morphostructural point of view using optical and scanning electron microscopy after thermal testing. The TPS composed of the carbon-felt-based ablative layer showed improved behaviour compared to the cork-based ablative ones in terms of the temperature increase rate during thermal conductivity testing, mass loss, as well as morphostructural appearance and material erosion after oxy-butane testing. The nSiC-based samples in both sets of TPSs showed improved behaviour compared to the un-filled ones, considering the temperature increase, mass loss, and morphostructure of the eroded material. Full article

(This article belongs to the Special Issue High-Temperature Composite Resin)

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16 pages, 13622 KiB

Open AccessArticle

Effect of Nano-Silica and Sorbitol on the Properties of Chitosan-Based Composite Films

by Wei Zhang, Wentao Zhou, Zisen Zhang, Di Zhang, Zhengzheng Guo, Penggang Ren and Fei Liu

Polymers 2023, 15(19), 4015; https://doi.org/10.3390/polym15194015 - 7 Oct 2023

Cited by 6 | Viewed by 1837

Abstract

Chitosan and its derivatives are widely used in food packaging, pharmaceutical, biotechnology, medical, textile, paper, agriculture, and environmental industries. However, the flexibility of chitosan films is extremely poor, which limits its relevant applications to a large extent. In this paper, chitosan/sorbitol/nano-silica (CS/sorbitol/SiO₂ [...] Read more.

Chitosan and its derivatives are widely used in food packaging, pharmaceutical, biotechnology, medical, textile, paper, agriculture, and environmental industries. However, the flexibility of chitosan films is extremely poor, which limits its relevant applications to a large extent. In this paper, chitosan/sorbitol/nano-silica (CS/sorbitol/SiO₂) composite films were prepared by the casting film method using chitosan, sorbitol, Tween-80 and nano-SiO₂ as raw materials. The structure of the films was characterized by infrared spectroscopy, electron scanning microscopy, and X-ray diffraction analysis. The effects of sorbitol and nano-silica dosage on the mechanical properties, thermal properties and water vapor barrier properties of the composite film were investigated. The results show that with the gradual increase in sorbitol (≤75 wt %), the elongation at the break of chitosan/sorbitol films significantly increased. When the addition of sorbitol was 75 wt %, the elongation at break of the chitosan/sorbitol composite film was 13 times higher than that of the chitosan film. Moreover, nano-SiO₂ can further improve the mechanical properties and thermal stability of the chitosan/sorbitol composite films. When the amount of nano-silica was 4.5 wt %, the composite film became more flexible, with a maximum elongation of 90.8% (which is 14 times that of chitosan film), and its toughness increased to 10.52 MJm⁻³ (which is 6 times that of chitosan film). This study balances the tensile strength and elongation at break of the composite films by adding a plasticizer and nano-filler, providing a reference for the preparation of chitosan composites or their blending with other polymers, and has practical guiding significance for the industrial production of biomass plastics. Full article

(This article belongs to the Section Polymer Membranes and Films)

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14 pages, 4265 KiB

Open AccessArticle

Enhancement of Mechanical Properties of Multilayer Ceramic Capacitors through a BaTiO₃/polydopamine Cover Layer

by Yong Park, Jung Jin Park, Kwan Soo Park, Yong Min Hong, Eun Jung Lee, Sang Ouk Kim and Jong Ho Lee

Polymers 2023, 15(19), 4014; https://doi.org/10.3390/polym15194014 - 7 Oct 2023

Cited by 1 | Viewed by 2069

Abstract

To fabricate multilayer ceramic capacitors (MLCCs) that can withstand external impacts, technologies to achieve excellent adhesion and mechanical strength of the cover layer should be essentially developed. Low adhesion and strength of the cover layer can lead to delamination and cracks in the [...] Read more.

To fabricate multilayer ceramic capacitors (MLCCs) that can withstand external impacts, technologies to achieve excellent adhesion and mechanical strength of the cover layer should be essentially developed. Low adhesion and strength of the cover layer can lead to delamination and cracks in the MLCC, respectively. In this study, we present a method for applying polydopamine (PDA), a mussel-inspired adhesive protein, for as robust cover layer on an MLCC. Barium titanate (BT) particles treated with PDA increase the dispersion stability of the BT/PDA slurry, preventing re-agglomeration of the particles and enhancing the adhesiveness and strength owing to the cohesive properties of PDA. Compared to the BT layer, the adhesion of the BT/PDA layer was significantly enhanced by 217%; consequently, the compression modulus of the BT/PDA cover layer increased by 29.4%. After firing, the N-doped graphitic PDA played an important role in producing an MLCC cover layer with increased hardness and toughness. Furthermore, the N-doped graphitic PDA with a hydrophobic surface forms tortuous moisture paths in the cover layer, preventing the degradation of insulation resistance of the MLCC. Full article

(This article belongs to the Section Polymer Membranes and Films)

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26 pages, 14828 KiB

Open AccessArticle

Effect of Salt Concentration on Oil Recovery during Polymer Flooding: Simulation Studies on Xanthan Gum and Gum Arabic

by Oluwasanmi Olabode, Oluwatimilehin Akinsanya, Olakunle Daramola, Akinleye Sowunmi, Charles Osakwe, Sarah Benjamin and Ifeanyi Samuel

Polymers 2023, 15(19), 4013; https://doi.org/10.3390/polym15194013 - 7 Oct 2023

Cited by 5 | Viewed by 1419

Abstract

Oil recoveries from medium and heavy oil reservoirs under natural recovery production are small because of the high viscosity of the oil. Normal water flooding procedures are usually ineffective, as the injected water bypasses much of the oil because of its high mobility. [...] Read more.

Oil recoveries from medium and heavy oil reservoirs under natural recovery production are small because of the high viscosity of the oil. Normal water flooding procedures are usually ineffective, as the injected water bypasses much of the oil because of its high mobility. Thermal flooding processes are desirable but have many disadvantages from costs, effects on the environment, and loss of lighter hydrocarbons. Chemical flooding options, such as bio-polymer flooding options, are attractive, as they are environmentally friendly and relatively cheap to deploy and help to increase the viscosity of the injecting fluid, thereby reducing its mobility and increasing its oil recovery. The downside to polymer flooding includes reservoir temperature, salinity, molecular weight, and composition. Six weight percentages of two polymers (xanthan gum, XG, and gum arabic, GA) are dissolved in water, and their viscosity is measured in the laboratory. These viscosities are incorporated with correlations in the Eclipse software to create models with different polymer concentrations of (0.1% wt., 0.2% wt., 0.3% wt., 0.4% wt., 0.5% wt., and 1% wt.). A base case of natural recovery and water injection was simulated to produce an oil recovery of 5.9% and 30.8%, respectively, while at 0.1% wt. and 1% wt., respectively, oil recoveries of 38.8% and 45.7% (for GA) and 48.1% and 49.8% (for XG) are estimated. At 5% and 10% saline conditions, a drop in oil recovery of (4.6% and 5.3%) is estimated during GA flooding and (1.2% and 1.7%) for XG flooding at 1% wt., respectively. XG exhibits higher oil recoveries compared to GA at the same % wt., while oil recoveries during GA floodings are more negatively affected by higher saline concentrations. Full article

(This article belongs to the Special Issue Advanced Polymer Composites in Oil Industry)

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11 pages, 3106 KiB

Open AccessArticle

Aerogel-Like Material Based on PEGylated Hyperbranched Polymethylethoxysiloxane

by Kirill Borisov, Alexandra Kalinina, Aleksandra Bystrova and Aziz Muzafarov

Polymers 2023, 15(19), 4012; https://doi.org/10.3390/polym15194012 - 7 Oct 2023

Viewed by 1504

Abstract

Aerogels are a class of materials that have gained increasing attention over the past several decades due to their exceptional physical and chemical properties. These materials are highly porous, with a low density and high surface area, allowing for applications such as insulation, [...] Read more.

Aerogels are a class of materials that have gained increasing attention over the past several decades due to their exceptional physical and chemical properties. These materials are highly porous, with a low density and high surface area, allowing for applications such as insulation, catalysis, and energy storage. However, traditional aerogels, such as pure silica aerogels, suffer from brittleness and fragility, which limit their usefulness in many applications. Herein, we have addressed this problem by using organosilicon compounds, namely polymethylsilsesquioxane derivatives, for the synthesis of aerogel-like materials. Specifically, we have developed a novel approach involving surfactant-free synthesis of microcapsules from partially PEGylated hyperbranched polymethylethoxysiloxane. Due to the highly diphilic nature of these compounds, they readily concentrate at the oil/water interface in aqueous emulsions encapsulating oil droplets. During the subsequent condensation, the organosilicon precursor is consumed for hexane encapsulation (yielding hollow microcapsules) followed by the formation of a continuous condensed phase. Concurrently, methyl groups ensure the hydrophobicity of the resulting materials, which eliminates the need of using additional reagents for their hydrophobization. Full article

(This article belongs to the Section Polymer Chemistry)

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11 pages, 3926 KiB

Open AccessArticle

Evaluation of the Anti-Inflammatory Pain Effect of Ginsenoside-Conjugated O-Carboxymethyl Chitosan Particles

by Huan-Jun Lu, Jian-Ke Cen, Yu Ren and Mei-Xian Li

Polymers 2023, 15(19), 4011; https://doi.org/10.3390/polym15194011 - 6 Oct 2023

Cited by 3 | Viewed by 1365

Abstract

Nanoparticle delivery of functional molecules or vaccines is an effective method for the treatment of many diseases. This study aims to design ginsenoside Rh2-conjugated O-carboxymethyl chitosan (O-CMC/Rh2) as a drug delivery system and explore its anti-nociceptive effects. O-CMC/Rh2 was synthesized with an esterification [...] Read more.

Nanoparticle delivery of functional molecules or vaccines is an effective method for the treatment of many diseases. This study aims to design ginsenoside Rh2-conjugated O-carboxymethyl chitosan (O-CMC/Rh2) as a drug delivery system and explore its anti-nociceptive effects. O-CMC/Rh2 was synthesized with an esterification reaction, and its chemical composition and morphology were evaluated using proton nuclear magnetic resonance (¹H NMR), the attenuated total reflectance-Fourier transform infrared (ATR-FTIR) spectroscopy, and scanning electron microscopy (SEM). In addition, the in vitro cumulative release of Rh2 from the O-CMC/Rh2 was also evaluated under different pH conditions. The results showed that the ginsenoside Rh2 was successfully conjugated to the O-CMC matrix and exhibited a highly porous structure after conjugation, facilitating the release of Rh2 from O-CMC. Complete Freund’s adjuvant (CFA) and burn injury-induced pain models were used to evaluate the anti-nociceptive effects of O-CMC/Rh2 on inflammatory pain. O-CMC/Rh2 reduced CFA-induced pain hypersensitivity in a dose-dependent manner and had a longer analgesic effect than Rh2. In addition, O-CMC/Rh2 also relieved the chronic pain induced by bury injury. These results indicated that O-CMC/Rh2 could be useful in reducing inflammatory pain, thus possessing a potential medicinal application in pain therapy. Full article

(This article belongs to the Special Issue Chitosan-Based Polymers as Promising Materials for a Variety of Biomedical Applications)

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18 pages, 1957 KiB

Open AccessArticle

Soybean-Based Polyol as a Substitute of Fossil-Based Polyol on the Synthesis of Thermoplastic Polyurethanes: The Effect of Its Content on Morphological and Physicochemical Properties

by Juliano R. Ernzen, José A. Covas, Angel Marcos-Fernández, Rudinei Fiorio and Otávio Bianchi

Polymers 2023, 15(19), 4010; https://doi.org/10.3390/polym15194010 - 6 Oct 2023

Cited by 1 | Viewed by 1646

Abstract

Thermoplastic polyurethanes (TPUs) are remarkably versatile polymers due to the wide range of raw materials available for their synthesis, resulting in physicochemical characteristics that can be tailored according to the specific requirements of their final applications. In this study, a renewable bio-based polyol [...] Read more.

Thermoplastic polyurethanes (TPUs) are remarkably versatile polymers due to the wide range of raw materials available for their synthesis, resulting in physicochemical characteristics that can be tailored according to the specific requirements of their final applications. In this study, a renewable bio-based polyol obtained from soybean oil is used for the synthesis of TPU via reactive extrusion, and the influence of the bio-based polyol on the multi-phase structure and properties of the TPU is studied. As raw materials, 4,4′-diphenylmethane (MDI), 1,4-butanediol, a fossil-based polyester polyol, and a bio-based polyol are used. The fossil-based to soybean-based polyol ratios studied are 100/0, 99/1, 95/5, 90/10, 80/20, and 50/50% by weight, respectively. The TPUs were characterized by size exclusion chromatography (SEC), gel content analysis, Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), small-angle X-ray scattering (SAXS), dynamic mechanical analysis (DMA), and contact angle measurements. The results reveal that incorporating the renewable polyol enhances the compatibility between the rigid and flexible segments of the TPU. However, due to its high functionality, the addition of soybean-based polyol can promote cross-linking. This phenomenon reduces the density of hydrogen bonds within the material, also reducing polarity and restricting macromolecular mobility, as corroborated by higher glass transition temperature (T_g) values. Remarkably, the addition of small amounts of the bio-based polyol (up to 5 wt.% of the total polyol content) results in high-molecular-weight TPUs with lower polarity, combined with suitable processability and mechanical properties, thus broadening the range of applications and improving their sustainability. Full article

(This article belongs to the Collection Polyurethanes)

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28 pages, 4938 KiB

Open AccessArticle

Migration Studies and Endocrine Disrupting Activities: Chemical Safety of Cosmetic Plastic Packaging

by Elias Bou-Maroun, Laurence Dahbi, Laurence Dujourdy, Pierre-Jacques Ferret and Marie-Christine Chagnon

Polymers 2023, 15(19), 4009; https://doi.org/10.3390/polym15194009 - 6 Oct 2023

Cited by 2 | Viewed by 2648

Abstract

The endocrine activity and endocrine disruptor (ED) chemical profiles of eleven plastic packaging materials covering five major polymer types (3PET, 1HDPE, 4LDPE, 2 PP, and 1SAN) were investigated using in vitro cell-based reporter-gene assays and a non-targeted chemical analysis using gas chromatography coupled [...] Read more.

The endocrine activity and endocrine disruptor (ED) chemical profiles of eleven plastic packaging materials covering five major polymer types (3PET, 1HDPE, 4LDPE, 2 PP, and 1SAN) were investigated using in vitro cell-based reporter-gene assays and a non-targeted chemical analysis using gas chromatography coupled to mass spectrometry (GC-MS). To mimic cosmetic contact, six simulants (acidic, alkaline, neutral water, ethanol 30%, glycerin, and paraffin) were used in migration assays performed by filling the packaging with simulant. After 1 month at 50 °C, simulants were concentrated by Solid Phase Extraction (SPE) or Liquid-Liquid Extraction (LLE). The migration profiles of seven major endocrine disrupting chemicals detected from GC-MS in the different materials and simulants were compared with Estrogen Receptor (ER) and Androgen Receptor (AR) activities. With low extraction of ED chemicals in aqueous simulants, no endocrine activities were recorded in the leachates. Paraffin was shown to be the most extracting simulant of antiandrogenic chemicals, while glycerin has estrogenic activities. Overall, ED chemical migration in paraffin was correlated with hormonal activity. The NIAS 2,4-di-tert-butyl phenol and 7,9-di-tert-butyl1-oxaspiro (4,5) deca-6,9-diene-2,8-dione were two major ED chemicals present in all polymers (principally in PP and PE) and in the highest quantity in paraffin simulant. The use of glycerin and liquid paraffin as cosmetic product simulants was demonstrated to be relevant and complementary for the safety assessment of released compounds with endocrine activities in this integrated strategy combining bioassays and analytical chemistry approaches. Full article

(This article belongs to the Section Polymer Applications)

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13 pages, 3082 KiB

Open AccessArticle

Mesostructured Fibrils Exfoliated in Deep Eutectic Solvent as Building Blocks of Collagen Membranes

by Ying Pei, Wei Li, Lu Wang, Jing Cui, Lu Li, Shengjie Ling, Keyong Tang and Huafeng Tian

Polymers 2023, 15(19), 4008; https://doi.org/10.3390/polym15194008 - 6 Oct 2023

Viewed by 1549

Abstract

The mesoscale components of collagen (nanofibrils, fibrils, and fiber bundles) are well organized in native tissues, resulting in superior properties and diverse functions. In this paper, we present a simple and controlled liquid exfoliation method to directly extract medium-sized collagen fibers ranging from [...] Read more.

The mesoscale components of collagen (nanofibrils, fibrils, and fiber bundles) are well organized in native tissues, resulting in superior properties and diverse functions. In this paper, we present a simple and controlled liquid exfoliation method to directly extract medium-sized collagen fibers ranging from 102 to 159 nm in diameter from bovine Achilles tendon using urea/hydrochloric acid and a deep eutectic solvent (DES). In situ observations under polarized light microscopy (POM) and molecular dynamics simulations revealed the effects of urea and GuHCl on tendon collagen. FTIR study results confirmed that these fibrils retained the typical structural characteristics of type I collagen. These shed collagen fibrils were then used as building blocks to create independent collagen membranes with good and stable mechanical properties, excellent barrier properties, and cell compatibility. A new method for collagen processing is provided in this work by using DES-assisted liquid exfoliation for constructing robust collagen membranes with mesoscale collagen fibrils as building blocks. Full article

(This article belongs to the Special Issue Advanced Biopolymer-Based Composites)

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15 pages, 5784 KiB

Open AccessReview

Exploring the Prospects of Macadamia Nutshells for Bio-Synthetic Polymer Composites: A Review

by Md Sefat Khan, Md Mainul Islam, Jayantha Epaarachchi and Shinichi Shibata

Polymers 2023, 15(19), 4007; https://doi.org/10.3390/polym15194007 - 6 Oct 2023

Cited by 1 | Viewed by 2265

Abstract

The global production of macadamia nuts has witnessed a significant increase, resulting in the accumulation of large quantities of discarded nutshells. These nutshells possess the properties of remarkable hardness and toughness, which are comparable to those of aluminum. Incorporating natural fillers to enhance [...] Read more.

The global production of macadamia nuts has witnessed a significant increase, resulting in the accumulation of large quantities of discarded nutshells. These nutshells possess the properties of remarkable hardness and toughness, which are comparable to those of aluminum. Incorporating natural fillers to enhance the properties of composite materials for various applications, including light duty, structural, and semi-structural purposes, is a common practice. Given their inherent hardness and toughness, macadamia nutshells present an intriguing choice as fillers, provided that the manufacturing conditions are economically viable. With the urgent need to shift toward natural fillers and reduce reliance on synthetics, exploring macadamia nutshells as components of natural fiber composites becomes imperative. This review aims to comprehensively examine the existing body of knowledge on macadamia nutshells and their bio-synthetic polymer composites, highlighting key research findings, achievements, and identifying knowledge gaps. Furthermore, the article will outline prospective areas of focus for future research endeavors in this domain, aligning with the universal goal of minimizing synthetic materials. Full article

(This article belongs to the Section Polymer Composites and Nanocomposites)

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19 pages, 7565 KiB

Open AccessArticle

Wettability and Frictional Studies of PEEK Composites against Co-Cr Alloys with Surface Textures

by Xifang Zhang, Zhenqiang Yao, Haifeng Du, Jiacheng Song, Zhiyi Jin and Wei Xu

Polymers 2023, 15(19), 4006; https://doi.org/10.3390/polym15194006 - 6 Oct 2023

Cited by 1 | Viewed by 1250

Abstract

With the aim of promoting the qualities for total hip joint replacement, the wettability and tribological behaviors of PEEK composites pins with two sets of different fillers (PEEK/CF or PEEK/CF/PTFE/graphite) against Co-Cr alloy discs with five categories of surface textures (polished, orthogonal, spiral, [...] Read more.

With the aim of promoting the qualities for total hip joint replacement, the wettability and tribological behaviors of PEEK composites pins with two sets of different fillers (PEEK/CF or PEEK/CF/PTFE/graphite) against Co-Cr alloy discs with five categories of surface textures (polished, orthogonal, spiral, r-θ, and orthogonal combined with spiral) were explored. It is revealed that the existence of CF in PEEK matrix increases the hydrophilicity in addition to the strength of PEEK, while the addition of PTFE increases the hydrophobicity of PEEK. The Co-Cr alloy discs with hydrophilic properties can be adjusted as hydrophobic, with the depth of textured grooves exceeding the critical sag height determined by the contact angle and the groove width. It can be concluded that PEEK/CF/PTFE/graphite composite has a lower wear rate than PEEK only reinforced with CF against Co-Cr alloy, both without surface texture and with shallow or deep grooves. The existence of shallow grooves on the disc surface could help the PEEK blends to achieve a steady friction against Co-Cr alloy in addition to collecting the worn debris. PEEK blend pins with 10 vol% CF, 10 vol% PTFE and 10 vol% graphite can achieve a lower friction coefficient of no more than 0.2 against Co-Cr alloy discs with shallow grooves around 3.5 μm in orthogonal or spiral textures. Full article

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13 pages, 2707 KiB

Open AccessArticle

Highly Efficient Flexible Roll-to-Roll Organic Photovoltaics Based on Non-Fullerene Acceptors

by Yu-Ching Huang, Hou-Chin Cha, Shih-Han Huang, Chia-Feng Li, Svette Reina Merden Santiago and Cheng-Si Tsao

Polymers 2023, 15(19), 4005; https://doi.org/10.3390/polym15194005 - 6 Oct 2023

Cited by 4 | Viewed by 1863

Abstract

The ability of organic photovoltaics (OPVs) to be deposited on flexible substrates by roll-to-roll (R2R) processes is highly attractive for rapid mass production. Many research teams have demonstrated the great potential of flexible OPVs. However, the fabrication of R2R-coated OPVs is quite limited. [...] Read more.

The ability of organic photovoltaics (OPVs) to be deposited on flexible substrates by roll-to-roll (R2R) processes is highly attractive for rapid mass production. Many research teams have demonstrated the great potential of flexible OPVs. However, the fabrication of R2R-coated OPVs is quite limited. There is still a performance gap between the R2R flexible OPVs and the rigid OPVs. In this study, we demonstrate the promising photovoltaic characteristics of flexible OPVs fabricated from blends of low bandgap polymer poly[(2,6-(4,8-bis(5-(2-ethylhexyl)thiophen-2-yl)-benzo[1,2-b:4,5-b′]dithiophene))-alt-(5,5-(1′,3′-di-2-thienyl-5′,7′-bis(2-ethylhexyl)benzo[1′,2′-c:4′,5′-c′]dithiophene-4,8-dione)] (PBDB-T) and non-fullerene 3,9-bis(2-methylene-(3-(1,1-dicyanomethylene)-indanone))-5,5,11,11-tetrakis(4-hexylphenyl)-dithieno[2,3-d:2′,3′-d′]-s-indaceno[1,2-b:5,6-b′]dithiophene (ITIC). We successfully R2R slot-die coated the flexible OPVs with high power conversion efficiency (PCE) of over 8.9% under irradiation of simulated sunlight. Our results indicate that the processing parameters significantly affect the PCE of R2R flexible OPVs. By adjusting the amount of solvent additive and processing temperature, as well as optimizing thermal annealing conditions, the high PCE of R2R slot-die coated OPVs can be obtained. These results provide significant insights into the fundamentals of highly efficient OPVs for the R2R slot-die coating process. Full article

(This article belongs to the Special Issue Polymer Films for Photovoltaic Applications II)

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