Journal Description
Polymers
Polymers
is an international, peer-reviewed, open access journal of polymer science published semimonthly online by MDPI. Belgian Polymer Group (BPG), European Colloid & Interface Society (ECIS), National Interuniversity Consortium of Materials Science and Technology (INSTM) and North American Thermal Analysis Society (NATAS) are affiliated with Polymers and their members receive a discount on the article processing charges.
- Open Access— free for readers, with article processing charges (APC) paid by authors or their institutions.
- High Visibility: indexed within Scopus, SCIE (Web of Science), Ei Compendex, PubMed, PMC, FSTA, CAPlus / SciFinder, Inspec, and other databases.
- Journal Rank: JCR - Q1 (Polymer Science) / CiteScore - Q1 (Polymers and Plastics)
- Rapid Publication: manuscripts are peer-reviewed and a first decision is provided to authors approximately 13.7 days after submission; acceptance to publication is undertaken in 2.9 days (median values for papers published in this journal in the second half of 2023).
- Recognition of Reviewers: reviewers who provide timely, thorough peer-review reports receive vouchers entitling them to a discount on the APC of their next publication in MDPI journals, in appreciation of the work.
- Testimonials: See what our authors and editors say about Polymers.
Impact Factor:
5.0 (2022);
5-Year Impact Factor:
5.0 (2022)
Latest Articles
How the Digital Product Passport Can Lead the Plastics Industry towards a Circular Economy—A Case Study from Bottle Caps to Frisbees
Polymers 2024, 16(10), 1420; https://doi.org/10.3390/polym16101420 (registering DOI) - 16 May 2024
Abstract
The Digital Product Passport (DPP) as a product-specific data set is a powerful tool that provides information on the origin or composition of products and increases transparency and traceability. This recycling case study accompanies the production of 2192 frisbees, which originated from collected
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The Digital Product Passport (DPP) as a product-specific data set is a powerful tool that provides information on the origin or composition of products and increases transparency and traceability. This recycling case study accompanies the production of 2192 frisbees, which originated from collected beverage bottle caps. In total, 486.7 kg of feedstock was collected and transformed into 363.2 kg of final product with verified traceability through all process steps via a DPP, provided by the R-Cycle initiative and based on the GS1 standard. This demanded a generally agreed dataset, the availability of technical infrastructure, and additional effort in the processing steps to collect and process the data. R-Cycle offers a one-layer DPP where the data structure is lean and information is visible to everyone. This is beneficial to a variety of stakeholders in terms of transparency. However, it does not allow the sharing of sensitive information. On the one hand, the DPP has a high potential to be an enabler for customer engagement, origin verification, or as a starting point for more efficient and advanced recycling of plastics. On the other hand, the DPP involves a certain effort in data generation and handling, which must be justified by the benefits. For small, simple packaging items, the DPP may not be the perfect solution for all problems. However, with a broader societal mindset and legislative push, the DPP can become a widely used and trusted declaration tool. This can support the plastics industry in its journey towards a circular economy.
Full article
(This article belongs to the Section Circular and Green Polymer Science)
Open AccessArticle
Progress toward the Definition of X-ray Computed Tomography Accuracy in the Characterization of Polymer-Based Lattice Structures
by
Daniel Gallardo, Lucía-Candela Díaz, José Antonio Albajez and José Antonio Yagüe-Fabra
Polymers 2024, 16(10), 1419; https://doi.org/10.3390/polym16101419 (registering DOI) - 16 May 2024
Abstract
Lattice structures have become an innovative solution for the improvement of part design, as they are able to substitute solid regions, maintain mechanical capabilities, and reduce material usage; however, dimensional quality control of these geometries is challenging. X-ray computed tomography (XCT) is the
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Lattice structures have become an innovative solution for the improvement of part design, as they are able to substitute solid regions, maintain mechanical capabilities, and reduce material usage; however, dimensional quality control of these geometries is challenging. X-ray computed tomography (XCT) is the most suitable non-destructive metrological technique as it is capable of characterizing internal features and hidden elements. Uncertainty estimation of XCT is still in development, and studies typically use high-resolution calibrated devices such as focal variation microscopes (FVMs) as a reference, focusing on certain parts of the lattice but not the whole structure. In this paper, an estimation of the accuracy of XCT evaluation of a complete lattice structure in comparison to a higher-resolution reference device (FVM) is presented. Experimental measurements are taken on ad hoc designed test objects manufactured in polyamide 12 (PA12) using selective laser sintering (SLS), optimized for the evaluation on both instruments using different cubic-based lattice typologies. The results confirm higher precision on XCT evaluation in both qualitative and quantitative analysis. Even with a lower resolution, XCT is able to characterize details of the surface such as re-entrant features; as well, standard deviations and uncertainties in strut diameter evaluation remain more stable in all cells in XCT, identifying on the other hand reconstruction problems on FVM measurements. Moreover, it is shown that, using XCT, no additional evaluation errors were found in inner cells, suggesting that the measurement of external elements could be representative of the whole structure for metrological purposes.
Full article
(This article belongs to the Special Issue Polymeric Materials in 3D Printing)
Open AccessArticle
Synthesis of Room Temperature Curable Polymer Binder Mixed with Polymethyl Methacrylate and Urethane Acrylate for High-Strength and Improved Transparency
by
Ju-Hong Lee, Won-Bin Lim, Jin-Gyu Min, Jae-Ryong Lee, Ju-Won Kim, Ji-Hong Bae and Pil-Ho Huh
Polymers 2024, 16(10), 1418; https://doi.org/10.3390/polym16101418 (registering DOI) - 16 May 2024
Abstract
Urethane acrylate (UA) was synthesized from various di-polyols, such as poly(tetrahydrofuran) (PTMG, Mn = 1000), poly(ethylene glycol) (PEG, Mn = 1000), and poly(propylene glycol) (PPG, Mn = 1000), for use as a polymer binder for paint. Polymethyl methacrylate (PMMA) and UA were blended
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Urethane acrylate (UA) was synthesized from various di-polyols, such as poly(tetrahydrofuran) (PTMG, Mn = 1000), poly(ethylene glycol) (PEG, Mn = 1000), and poly(propylene glycol) (PPG, Mn = 1000), for use as a polymer binder for paint. Polymethyl methacrylate (PMMA) and UA were blended to form an acrylic resin with high transmittance and stress-strain curve. When PMMA was blended with UA, a network structure was formed due to physical entanglement between the two polymers, increasing the mechanical properties. UA was synthesized by forming a prepolymer using di-polyol and hexamethylene diisocyanate, which were chain structure monomers, and capping them with 2-hydroxyethyl methacrylate to provide an acryl group. Fourier transform infrared spectroscopy was used to observe the changes in functional groups, and gel permeation chromatography was used to confirm that the three series showed similar molecular weight and PDI values. The yellowing phenomenon that appears mainly in the curing reaction of the polymer binder was solved, and the mechanical properties according to the effects of the polyol used in the main chain were compared. The content of the blended UA was quantified using ultravioletvisible spectroscopy at a wavelength of 370 nm based on 5, 10, 15, and 20 wt%, and the shear strength and tensile strength were evaluated using specimens in a suitable mode. The ratio for producing the polymer binder was optimized. The mechanical properties of the polymer binder with 5–10 wt% UA were improved in all series.
Full article
(This article belongs to the Special Issue Progress in Polyurethane and Composites)
Open AccessArticle
Numerical Simulation of Mold Filling of Polymeric Materials with Friction Effect during Hot Embossing Process at Micro Scale
by
Faleh Rabhi, Gang Cheng and Thierry Barriere
Polymers 2024, 16(10), 1417; https://doi.org/10.3390/polym16101417 (registering DOI) - 16 May 2024
Abstract
The filling efficiency during the hot embossing process at micro scale is essential for micro-component replication. The presence of the unfilled area is often due to the inadequate behavior law applied to the embossed materials. This research consists of the identification of viscoplastic
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The filling efficiency during the hot embossing process at micro scale is essential for micro-component replication. The presence of the unfilled area is often due to the inadequate behavior law applied to the embossed materials. This research consists of the identification of viscoplastic law (two-layer viscoplastic model) of polymers and the optimization of processing parameters. Mechanical tests have been performed for two polymers at 20 °C and 30 °C above their glass transition temperature. The viscoplastic parameters are characterized based on stress–strain curves from the compression tests. The influences of imposed displacement, temperature, and friction on mold filling are investigated. The processing parameters are optimized to achieving the complete filling of micro cavities. The replication of a micro-structured cavity has been effectuated using this process and the experimental observations validate the results in the simulation, which confirms the efficiency of the proposed numerical approach.
Full article
(This article belongs to the Section Polymer Processing and Engineering)
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Open AccessArticle
Polydimethylsiloxane Surface Modification of Microfluidic Devices for Blood Plasma Separation
by
Margarida Gonçalves, Inês Maia Gonçalves, Joel Borges, Vera Faustino, Delfim Soares, Filipe Vaz, Graça Minas, Rui Lima and Diana Pinho
Polymers 2024, 16(10), 1416; https://doi.org/10.3390/polym16101416 (registering DOI) - 16 May 2024
Abstract
Over the last decade, researchers have developed a variety of new analytical and clinical diagnostic devices. These devices are predominantly based on microfluidic technologies, where biological samples can be processed and manipulated for the collection and detection of important biomolecules. Polydimethylsiloxane (PDMS) is
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Over the last decade, researchers have developed a variety of new analytical and clinical diagnostic devices. These devices are predominantly based on microfluidic technologies, where biological samples can be processed and manipulated for the collection and detection of important biomolecules. Polydimethylsiloxane (PDMS) is the most commonly used material in the fabrication of these microfluidic devices. However, it has a hydrophobic nature (contact angle with water of 110°), leading to poor wetting behavior and issues related to the mixing of fluids, difficulties in obtaining uniform coatings, and reduced efficiency in processes such as plasma separation and molecule detection (protein adsorption). This work aimed to consider the fabrication aspects of PDMS microfluidic devices for biological applications, such as surface modification methods. Therefore, we studied and characterized two methods for obtaining hydrophilic PDMS surfaces: surface modification by bulk mixture and the surface immersion method. To modify the PDMS surface properties, three different surfactants were used in both methods (Pluronic® F127, polyethylene glycol (PEG), and polyethylene oxide (PEO)) at different percentages. Water contact angle (WCA) measurements were performed to evaluate the surface wettability. Additionally, capillary flow studies were performed with microchannel molds, which were produced using stereolithography combined with PDMS double casting and replica molding procedures. A PDMS microfluidic device for blood plasma separation was also fabricated by soft lithography with PDMS modified by PEO surfactant at 2.5% (v/v), which proved to be the best method for making the PDMS hydrophilic, as the WCA was lower than 50° for several days without compromising the PDMS’s optical properties. Thus, this study indicates that PDMS surface modification shows great potential for enhancing blood plasma separation efficiency in microfluidic devices, as it facilitates fluid flow, reduces cell aggregations and the trapping of air bubbles, and achieves higher levels of sample purity.
Full article
(This article belongs to the Special Issue Advanced Polymer Composite Materials: Processing, Modeling, Properties and Applications III)
Open AccessArticle
Evaluating the Effects of Metallic Waste on the Structural and Gamma-Ray Shielding Properties of Epoxy Composites
by
Sitah Alanazi, Mohammad Hanfi, Mohammad W. Marashdeh, Mamduh J. Aljaafreh and Karem A. Mahmoud
Polymers 2024, 16(10), 1415; https://doi.org/10.3390/polym16101415 (registering DOI) - 16 May 2024
Abstract
The objective of the research is to develop novel materials that are both inexpensive and have a low density, while also being able to endure the transportation of γ-photons with low-to-medium energy levels. The outcome consisted of four epoxy resins that were strengthened
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The objective of the research is to develop novel materials that are both inexpensive and have a low density, while also being able to endure the transportation of γ-photons with low-to-medium energy levels. The outcome consisted of four epoxy resins that were strengthened with different quantities of heavy metallic waste. The density of the formed composites improved from 1.134 ± 0.022 g/cm3 to 1.560 ± 0.0312 g/cm3 when the waste content was raised from 0 to 40 weight percent. The theoretical investigation was determined using Monte Carlo (MCNP) simulation software, and the results of linear attenuation coefficient were justified experimentally in a low and medium energy range of 15–662 keV. The mass attenuation coefficient results in a low gamma energy range (15–122 keV) varied in between 3.175 and 0.159 cm2/g (for E-MW0 composite) and in between 8.212 and 0.164 cm2/g (for E-MW40 composite). The decrease in mass attenuation coefficient was detected in a medium gamma photon energy range (122–662 keV) with 0.123–0.082 cm2/g (for E-MW0 composite) and 0.121–0.080 cm2/g (for E-MW40 composite). The density of the enhanced composites influenced these parameters. As the metallic waste composition increased, the fabricated composites’ half-value thickness decreased. At 15 keV, the half-value thickness decreased from 0.19 to 0.05 cm. At 59 keV, it fell from 2.70 to 1.41 cm. At 122 keV, it fell from 3.90 to 2.72 cm. At 662 keV, it fell from 7.45 to 5.56 cm. This decrease occurred as the heavy metal waste concentration increased from 0 to 40 wt.%. The study indicates that as metallic waste concentrations rise, there is a rise in the effective atomic number and a decline in the buildup factors.
Full article
(This article belongs to the Special Issue Resin-Based Polymer Materials and Related Applications: Volume 2)
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Open AccessArticle
Biomass Waste Utilization as Nanocomposite Anodes through Conductive Polymers Strengthened SiO2/C from Streblus asper Leaves for Sustainable Energy Storages
by
Thanapat Autthawong, Natthakan Ratsameetammajak, Kittiched Khunpakdee, Mitsutaka Haruta, Torranin Chairuangsri and Thapanee Sarakonsri
Polymers 2024, 16(10), 1414; https://doi.org/10.3390/polym16101414 - 16 May 2024
Abstract
Sustainable anode materials, including natural silica and biomass-derived carbon materials, are gaining increasing attention in emerging energy storage applications. In this research, we highlighted a silica/carbon (SiO2/C) derived from Streblus asper leaf wastes using a simple method. Dried Streblus asper leaves,
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Sustainable anode materials, including natural silica and biomass-derived carbon materials, are gaining increasing attention in emerging energy storage applications. In this research, we highlighted a silica/carbon (SiO2/C) derived from Streblus asper leaf wastes using a simple method. Dried Streblus asper leaves, which have plenty of biomass in Thailand, have a unique leaf texture due to their high SiO2 content. We can convert these worthless leaves into SiO2/C nanocomposites in one step, producing eco-materials with distinctive microstructures that influence electrochemical energy storage performance. Through nanostructured design, SiO2/C is thoroughly covered by a well-connected framework of conductive hybrid polymers based on the sodium alginate–polypyrrole (SA-PPy) network, exhibiting impressive morphology and performance. In addition, an excellent electrically conductive SA-PPy network binds to the SiO2/C particle surface through crosslinker bonding, creating a flexible porous space that effectively facilitates the SiO2 large volume expansion. At a current density of 0.3 C, this synthesized SA-PPy@Nano-SiO2/C anode provides a high specific capacity of 756 mAh g−1 over 350 cycles, accounting for 99.7% of the theoretical specific capacity. At the high current of 1 C (758 mA g−1), a superior sustained cycle life of over 500 cycles was evidenced, with over 93% capacity retention. The research also highlighted the potential for this approach to be scaled up for commercial production, which could have a significant impact on the sustainability of the lithium-ion battery industry. Overall, the development of green nanocomposites along with polymers having a distinctive structure is an exciting area of research that has the potential to address some of the key challenges associated with lithium-ion batteries, such as capacity degradation and safety concerns, while also promoting sustainability and reducing environmental impact.
Full article
(This article belongs to the Special Issue Carbon/Polymer Composite Materials)
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Open AccessArticle
Preparation of Polyaniline-Modified Cellulose/PDMS Composite Triboelectric Material and Application of Its Pretreatment in MOW Pulp
by
Xiaoping Sun, Yuhe Wei, Yanfen Sun, Juan Yuan, Haoqiu Chen, Zhuo Chen, Mengyang Wang and Lianxin Luo
Polymers 2024, 16(10), 1413; https://doi.org/10.3390/polym16101413 - 16 May 2024
Abstract
Self-powered electronic equipment has rapidly developed in the fields of sensing, motion monitoring, and energy collection, posing a greater challenge to triboelectric materials. Triboelectric materials need to enhance their electrical conductivity and mechanical strength to address the increasing demand for stability and to
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Self-powered electronic equipment has rapidly developed in the fields of sensing, motion monitoring, and energy collection, posing a greater challenge to triboelectric materials. Triboelectric materials need to enhance their electrical conductivity and mechanical strength to address the increasing demand for stability and to mitigate unpredictable physical damage. In this study, polyaniline-modified cellulose was prepared by means of in situ polymerization and compounded with polydimethylsiloxane, resulting in a triboelectric material with enhanced strength and conductivity. The material was fabricated into a tubular triboelectric nanogenerator (TENG) (G-TENG), and an electrocatalytic pretreatment of mixed office waste paper (MOW) pulp was performed using papermaking white water as the flowing liquid to improve the deinking performance. The electrical output performance of G-TENG is highest at a flow rate of 400 mL/min, producing a voltage of 22.76 V and a current of 1.024 μA. Moreover, the deinking effect of MOW was enhanced after the electrical pretreatment. This study explores the potential application of G-TENG as a self-powered sensor power supply and emphasizes its prospect as an energy collection device.
Full article
(This article belongs to the Special Issue Cellulose and Its Derivatives: Applications, and Future Perspectives II)
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Open AccessArticle
Optimizing Transport Carrier Free All-Polymer Solar Cells for Indoor Applications: TCAD Simulation under White LED Illumination
by
Marwa S. Salem, Mohamed Okil, Ahmed Shaker, Mohamed Abouelatta, Arwa N. Aledaily, Kawther A. Al-Dhlan, Mohammad T. Alshammari, Mostafa M. Salah and Mona El Sabbagh
Polymers 2024, 16(10), 1412; https://doi.org/10.3390/polym16101412 - 16 May 2024
Abstract
This work inspects the utilization of all-polymer solar cells (APSCs) in indoor applications under LED illumination, with a focus on boosting efficiency through simulation-based design. The study employs a SCAPS TCAD device simulator to investigate the performance of APSCs under white LED illumination
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This work inspects the utilization of all-polymer solar cells (APSCs) in indoor applications under LED illumination, with a focus on boosting efficiency through simulation-based design. The study employs a SCAPS TCAD device simulator to investigate the performance of APSCs under white LED illumination at 1000 lux, with a power density of 0.305 mW/cm2. Initially, the simulator is validated against experimental results obtained from a fabricated cell utilizing CD1:PBN-21 as an absorber blend and PEDOT:PSS as a hole transportation layer (HTL), where the initial measured efficiency is 16.75%. The simulation study includes an examination of both inverted and conventional cell structures. In the conventional structure, where no electron transportation layer (ETL) is present, various materials are evaluated for their suitability as the HTL. NiO emerges as the most promising HTL material, demonstrating the potential to achieve an efficiency exceeding 27%. Conversely, in the inverted configuration without an HTL, the study explores different ETL materials to engineer the band alignment at the interface. Among the materials investigated, ZnS emerges as the optimal choice, recording an efficiency of approximately 33%. In order to reveal the efficiency limitations of these devices, the interface and bulk defects are concurrently investigated. The findings of this study underscore the significance of careful material selection and structural design in optimizing the performance of APSCs for indoor applications.
Full article
(This article belongs to the Special Issue Application of Polymer Materials in Optoelectronic Devices)
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Open AccessArticle
Biodegradation of Polyurethane by Fungi Isolated from Industrial Wastewater—A Sustainable Approach to Plastic Waste Management
by
Aiswarya Rajan, Fuad Ameen, Ranjitha Jambulingam and Vijayalakshmi Shankar
Polymers 2024, 16(10), 1411; https://doi.org/10.3390/polym16101411 - 16 May 2024
Abstract
Polyurethane (PU) is a type of polymer, which exists in various forms in the environment. Very few studies are available concerning the structure or enzymatic mechanism of the microbial community, which can degrade PU. Degradation of PU remains a difficult problem with respect
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Polyurethane (PU) is a type of polymer, which exists in various forms in the environment. Very few studies are available concerning the structure or enzymatic mechanism of the microbial community, which can degrade PU. Degradation of PU remains a difficult problem with respect to the environmental and biological disciplines. This study mainly focused on identifying the micro-organisms able to degrade polyurethane and confirming the degradation by performing a plate assay, Sturm test and scanning electron microscopy. Optimal culture conditions for maximum PU degradation were also analyzed through classical methods. A soil burial test was conducted by placing polyurethane films in the soil for one month, and the microbe growing on the surface of polyurethane films—with a maximum degradation of 55%—was isolated and identified as Aspergillus versicolor (ARF5). The culture medium was also optimized with different physical and chemical parameters for maximum PU degradation. The presence of CO2 as a by-product of PU biodegradation was confirmed through the Sturm test.
Full article
(This article belongs to the Section Biomacromolecules, Biobased and Biodegradable Polymers)
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Open AccessArticle
Preparation of UV Topcoat Microcapsules and Their Effect on the Properties of UV Topcoat Paint Film
by
Yongxin Xia and Xiaoxing Yan
Polymers 2024, 16(10), 1410; https://doi.org/10.3390/polym16101410 - 16 May 2024
Abstract
An orthogonal experiment was designed to prepare different UV topcoat microcapsules by adjusting the mass ratio of wall material to core material, HLB value of emulsifier, reaction temperature, and reaction time of UV topcoat microcapsule. By testing the morphology and multiple properties of
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An orthogonal experiment was designed to prepare different UV topcoat microcapsules by adjusting the mass ratio of wall material to core material, HLB value of emulsifier, reaction temperature, and reaction time of UV topcoat microcapsule. By testing the morphology and multiple properties of UV topcoat microcapsules, it was found that the biggest factor affecting the synthesis of UV topcoat microcapsules is the emulsifier HLB value. In order to further optimize the performance of UV topcoat microcapsules, a single-factor experiment was conducted with the emulsifier HLB value as the variable, and it was found that the UV topcoat microcapsules achieved the best performance when the emulsifier HLB value was 10.04. The optimal UV topcoat microcapsules were added to the UV topcoat at different amounts to prepare UV topcoat paint films. Through testing the various properties of the UV topcoat paint film, it was determined that the performance of the UV topcoat paint film was optimal when the amount of UV topcoat microcapsules added to the UV topcoat was 4.0%. The optical properties of the UV topcoat paint film were tested, and the effect of UV topcoat microcapsules on the color difference and glossiness of the UV topcoat paint film was not significant. The tensile and self-healing performance of UV topcoat microcapsules were tested. UV topcoat microcapsules can enhance the toughness of the UV topcoat paint film to a certain extent, suppress the generation of microcracks, and have a good self-healing effect. The results provide experimental support for the preparation of microcapsules using UV coatings as core materials for the self-healing of UV coatings.
Full article
(This article belongs to the Special Issue Polymer Coatings for High-Performance Applications)
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Open AccessArticle
Facile Fabrication of Highly Efficient Chitosan-Based Multifunctional Coating for Cotton Fabrics with Excellent Flame-Retardant and Antibacterial Properties
by
Yuan-Yuan Huang, Li-Ping Zhang, Xing Cao, Xin-Yu Tian and Yan-Peng Ni
Polymers 2024, 16(10), 1409; https://doi.org/10.3390/polym16101409 - 16 May 2024
Abstract
Interest in the development of eco-friendly, sustainable, and convenient bio-based coatings to enhance flame retardancy and antibacterial properties in cotton fabrics is growing. In this work, chitosan was protonated at its amino groups using a method with a high atom economy using an
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Interest in the development of eco-friendly, sustainable, and convenient bio-based coatings to enhance flame retardancy and antibacterial properties in cotton fabrics is growing. In this work, chitosan was protonated at its amino groups using a method with a high atom economy using an equimolar amount of amino trimethylene phosphonic acid (ATMP), resulting in the fabrication of a single-component chitosan-based multifunctional coating (ATMP-CS), thereby avoiding any additional neutralization or purification steps. Cotton fabrics coated with various loads of ATMP-CS were prepared through a padding–drying–curing process. The morphology, thermal stability, mechanical properties, antibacterial properties, flame-retardant behavior, and flame-retardant mechanism of these fabrics were investigated. The coating exhibited excellent film-forming properties, and it imparted a uniform protective layer onto the surfaces of the cotton fabrics. When the load capacity reached 11.5%, the coated fabrics achieved a limiting oxygen index of 29.7% and successfully passed the VFT test. Moreover, the ATMP-CS coating demonstrated antibacterial rates against Escherichia coli and Staphylococcus aureus reaching 95.1% and 99.9%, respectively. This work presents a straightforward and gentle approach to fabricating colorless, environmentally friendly, and highly efficient fabric coatings that have potential applications in promoting the use of bio-based materials.
Full article
(This article belongs to the Special Issue Green Flame-Retardant Polymer Material)
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Open AccessReview
Modern Trends in Polymerization-Induced Self-Assembly
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Natalia S. Serkhacheva, Nickolay I. Prokopov, Evgenii A. Lysenko, Elena Yu. Kozhunova and Elena V. Chernikova
Polymers 2024, 16(10), 1408; https://doi.org/10.3390/polym16101408 - 15 May 2024
Abstract
Polymerization-induced self-assembly (PISA) is a powerful and versatile technique for producing colloidal dispersions of block copolymer particles with desired morphologies. Currently, PISA can be carried out in various media, over a wide range of temperatures, and using different mechanisms. This method enables the
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Polymerization-induced self-assembly (PISA) is a powerful and versatile technique for producing colloidal dispersions of block copolymer particles with desired morphologies. Currently, PISA can be carried out in various media, over a wide range of temperatures, and using different mechanisms. This method enables the production of biodegradable objects and particles with various functionalities and stimuli sensitivity. Consequently, PISA offers a broad spectrum of potential commercial applications. The aim of this review is to provide an overview of the current state of rational synthesis of block copolymer particles with diverse morphologies using various PISA techniques and mechanisms. The discussion begins with an examination of the main thermodynamic, kinetic, and structural aspects of block copolymer micellization, followed by an exploration of the key principles of PISA in the formation of gradient and block copolymers. The review also delves into the main mechanisms of PISA implementation and the principles governing particle morphology. Finally, the potential future developments in PISA are considered.
Full article
(This article belongs to the Special Issue Recent Advances in the Self-Assembly of Block Copolymers)
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Open AccessReview
Literature Review on Conjugated Polymers as Light-Sensitive Materials for Photovoltaic and Light-Emitting Devices in Photonic Biomaterial Applications
by
Paolo Coghi and Carmine Coluccini
Polymers 2024, 16(10), 1407; https://doi.org/10.3390/polym16101407 - 15 May 2024
Abstract
Due to their extended p-orbital delocalization, conjugated polymers absorb light in the range of visible–NIR frequencies. We attempt to exploit this property to create materials that compete with inorganic semiconductors in photovoltaic and light-emitting materials. Beyond competing for applications in photonic devices, organic
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Due to their extended p-orbital delocalization, conjugated polymers absorb light in the range of visible–NIR frequencies. We attempt to exploit this property to create materials that compete with inorganic semiconductors in photovoltaic and light-emitting materials. Beyond competing for applications in photonic devices, organic conjugated compounds, polymers, and small molecules have also been extended to biomedical applications like phototherapy and biodetection. Recent research on conjugated polymers has focused on bioapplications based on the absorbed light energy conversions in electric impulses, chemical energy, heat, and light emission. In this review, we describe the working principles of those photonic devices that have been applied and researched in the field of biomaterials.
Full article
(This article belongs to the Topic Conjugated Polymers: Preparation, Properties and Applications)
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Open AccessArticle
Effects of Curing Defects in Adhesive Layers on Carbon Fiber–Quartz Fiber Bonded Joint Performance
by
Xiaobo Yang, Miaomiao Zhang, Lihua Zhan, Bolin Ma, Xintong Wu, Cong Liu and He Xiang
Polymers 2024, 16(10), 1406; https://doi.org/10.3390/polym16101406 - 15 May 2024
Abstract
Due to their mechanical load-bearing and functional wave transmission, adhesively bonded joints of carbon fiber–quartz fiber composites have been widely used in the new generation of stealth aviation equipment. However, the curing defects, caused by deviations between the process environment and the setting
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Due to their mechanical load-bearing and functional wave transmission, adhesively bonded joints of carbon fiber–quartz fiber composites have been widely used in the new generation of stealth aviation equipment. However, the curing defects, caused by deviations between the process environment and the setting parameters, directly affect the service performance of the joint during the curing cycle. Therefore, the thermophysical parameter evolution of adhesive films was analyzed via dynamic DSC (differential scanning calorimeter), isothermal DSC and TGA (thermal gravimetric analyzer) tests. The various prefabricating defects within the adhesive layer were used to systematically simulate the impacts of void defects on the tensile properties, and orthogonal tests were designed to clarify the effects of the curing process parameters on the joints’ bonding performance. The results demonstrate that the J-116 B adhesive film starts to cure at a temperature of 160 °C and gradually forms a three-dimensional mesh-bearing structure. Furthermore, a bonding interface between the J-116 B adhesive film and the components to be connected is generated. When the curing temperature exceeds 200 °C, both the adhesive film and the resin matrix thermally degrade the molecular structure. The adhesive strength weakens with an increasing defect area ratio and number, remaining more sensitive to triangle, edge and penetration defects. By affecting the molecular structure of the adhesive film, the curing temperature has a significant impact on the bonding properties; when the curing degree is ensured, the curing pressure directly impacts the adhesive’s performance by influencing the morphology, number and distribution of voids. Conversely, the heating rate and heat preservation time have minimal effects on the bonding performance.
Full article
(This article belongs to the Special Issue Fiber-Reinforced Polymer Composites: Progress and Prospects)
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Open AccessReview
Polyglycerol Sebacate Elastomer: A Critical Overview of Synthetic Methods and Characterisation Techniques
by
Mariella Rosalia, Davide Rubes, Massimo Serra, Ida Genta, Rossella Dorati and Bice Conti
Polymers 2024, 16(10), 1405; https://doi.org/10.3390/polym16101405 - 15 May 2024
Abstract
Poly (glycerol sebacate) is a widely studied elastomeric copolymer obtained from the polycondensation of two bioresorbable monomers, glycerol and sebacic acid. Due to its biocompatibility and the possibility to tailor its biodegradability rate and mechanical properties, PGS has gained lots of interest in
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Poly (glycerol sebacate) is a widely studied elastomeric copolymer obtained from the polycondensation of two bioresorbable monomers, glycerol and sebacic acid. Due to its biocompatibility and the possibility to tailor its biodegradability rate and mechanical properties, PGS has gained lots of interest in the last two decades, especially in the soft tissue engineering field. Different synthetic approaches have been proposed, ranging from classic thermal polyesterification and curing to microwave-assisted organic synthesis, UV crosslinking and enzymatic catalysis. Each technique, characterized by its advantages and disadvantages, can be tailored by controlling the crosslinking density, which depends on specific synthetic parameters. In this work, classic and alternative synthetic methods, as well as characterisation and tailoring techniques, are critically reviewed with the aim to provide a valuable tool for the reproducible and customized production of PGS for tissue engineering applications.
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(This article belongs to the Special Issue Biocompatible Polymers for Tissue Engineering and Drug Delivery)
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Biodegradation of Polystyrene by Plastic-Eating Tenebrionidae Larvae
by
Erika Alessia Di Liberto, Giuseppe Battaglia, Rosalia Pellerito, Giusy Curcuruto and Nadka Tz. Dintcheva
Polymers 2024, 16(10), 1404; https://doi.org/10.3390/polym16101404 - 15 May 2024
Abstract
Polystyrene (PS) is an extremely stable polymer with a relatively high molecular weight and a strong hydrophobic character that makes it highly resistant to biodegradation. In this study, PS was subjected to biodegradation tests by Tenebrio Molitor (T. Molitor) and Zophobas Morio
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Polystyrene (PS) is an extremely stable polymer with a relatively high molecular weight and a strong hydrophobic character that makes it highly resistant to biodegradation. In this study, PS was subjected to biodegradation tests by Tenebrio Molitor (T. Molitor) and Zophobas Morio (Z. Morio) larvae. Specifically, six different experimental diets were compared: (i) T. Molitor fed with bran; (ii) T. Molitor fed only PS; (iii) T. Molitor fed only PS treated with H2O2; (iv) Z. Morio fed with bran; (v) Z. Morio fed only PS; and (vi) Z. Morio fed only PS treated with H2O2. Therefore, the mass change of the larvae and the survival rate were measured periodically, while the frass collected after 15 and 30 days was analyzed by different analyses, such as spectroscopy (FTIR), spectrometry (molecular weight and polydispersity), thermal analysis (TGA) and microscopy (scanning electron microscopy observations). The obtained results suggest that in the case of T. Molitor larvae, larvae feeding on bran showed the highest survival rate of ~94% at 30 days, while in the case of the Z. Morio larvae, the highest survival rate was exhibited by larvae eating PS-H2O2. Although not strongly pronounced, the Mw and Mn of PS in the frass of both T. Molitor and Z. Morio larvae decreased over 30 days, suggesting PS biodegradation. Finally, the morphological analysis shows that PS samples isolated from the frass of T. Molitor and Z. Morio larvae showed completely different, rough and irregularly carved surface structures, in comparison to PS before biodegradation.
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(This article belongs to the Section Circular and Green Polymer Science)
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Differential Studies on the Structure of Lignin–Carbohydrate Complexes (LCC) in Alkali-Extracted Plant Hemicelluloses
by
Shuyu Pang, Xin Wang, Jiali Pu, Chen Liang, Shuangquan Yao and Chengrong Qin
Polymers 2024, 16(10), 1403; https://doi.org/10.3390/polym16101403 - 15 May 2024
Abstract
Hemicellulose extracted by alkali treatment is of interest because of the advantages of its intact sugar structure and high degree of polymerization. However, the hemicellulose extracted by alkali treatment contained more lignin fragments and the presence of a lignin–carbohydrate complex (LCC), which affected
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Hemicellulose extracted by alkali treatment is of interest because of the advantages of its intact sugar structure and high degree of polymerization. However, the hemicellulose extracted by alkali treatment contained more lignin fragments and the presence of a lignin–carbohydrate complex (LCC), which affected the isolation and purification of hemicellulose and its comprehensive utilization. Therefore, the evaluation of the LCC structure of different types of lignocellulosic resources is of great significance. In this study, the LCC structures of hardwoods and Gramineae were enriched in alkaline systems. Information on the composition, structural proportions, and connection patterns of LCC samples was discussed. The similarities and differences between the LCC structures of different units of raw materials were comparatively studied. The results indicated that the monosaccharide fractions were higher in the LCC of Gramineae compared to hardwoods. The composition of the lignin fraction was dominated by G and S units. The phenyl glycosidic (PhGlc) bond is the predominant LCC linkage under alkali-stabilized conditions. In addition, Gramineae PhGlc types are more numerous compared to hardwoods. The results of the study provide insights into the differences in the chemical composition and structural features of LCC in different plants and provide important guidance for the optimization of the process of purifying hemicellulose.
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(This article belongs to the Special Issue Carbohydrate Polymers: Synthesis, Preparation, Structural Characteristics and Applications)
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Pinecone-Inspired Humidity-Responsive Paper Actuators with Bilayer Structure
by
David Seelinger, Hussam Georges, Jan-Lukas Schäfer, Jasmin Huong, Rena Tajima, Christan Mittelstedt and Markus Biesalski
Polymers 2024, 16(10), 1402; https://doi.org/10.3390/polym16101402 - 15 May 2024
Abstract
Many plant materials in nature have the ability to change their shape to respond to external stimuli, such as humidity or moisture, to ensure their survival or safe seed release. A well-known example for this phenomenon is the pinecone, which is able to
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Many plant materials in nature have the ability to change their shape to respond to external stimuli, such as humidity or moisture, to ensure their survival or safe seed release. A well-known example for this phenomenon is the pinecone, which is able to open its scales at low humidity due to the specific bilayer structures of the scale. Inspired by this, we developed a novel humidity-driven actuator based on paper. This was realized by the lamination of untreated paper made from eucalyptus fibers to a paper–carboxymethyl cellulose (CMC) composite. As observed, the hygroexpansion of the composite can be easily controlled by the amount of CMC in the impregnated paper sheet, which, thus, controls the morphologic deformation of the paper bilayer. For a more detailed understanding of these novel paper soft robots, we also studied the dynamic water vapor adsorption, polymer distribution and hygroexpansion of the paper–polymer composites. Finally, we applied a geometrically nonlinear finite element model to predict the bending behavior of paper bilayers and compared the results to experimental data. From this, we conclude that due to the complexity of structure of the paper composite, a universal prediction of the hygromorphic behavior is not a trivial matter.
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(This article belongs to the Special Issue Advances in Cellulose-Based Polymers and Composites)
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Revisit of Polyaniline as a High-Capacity Organic Cathode Material for Li-Ion Batteries
by
Ruirui Zhao, Zu Chang, Xudong Fu, Mingli Xu, Xinping Ai and Jiangfeng Qian
Polymers 2024, 16(10), 1401; https://doi.org/10.3390/polym16101401 - 14 May 2024
Abstract
Polyaniline (PANI) has long been explored as a promising organic cathode for Li-ion batteries. However, its poor electrochemical utilization and cycling instability cast doubt on its potential for practical applications. In this work, we revisit the electrochemical performance of PANI in nonaqueous electrolytes,
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Polyaniline (PANI) has long been explored as a promising organic cathode for Li-ion batteries. However, its poor electrochemical utilization and cycling instability cast doubt on its potential for practical applications. In this work, we revisit the electrochemical performance of PANI in nonaqueous electrolytes, and reveal an unprecedented reversible capacity of 197.2 mAh g−1 (244.8 F g−1) when cycled in a wide potential range of 1.5 to 4.4 V vs. Li+/Li. This ultra-high capacity derives from 70% -NH- transformed to =NH+- during deep charging/discharging process. This material also demonstrates a high average coulombic efficiency of 98%, an excellent rate performance with 73.5 mAh g−1 at 1800 mA g−1, and retains 76% of initial value after 100 cycles, which are among the best reported values for PANI electrodes in battery applications.
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(This article belongs to the Special Issue State of the Art and Perspectives of Polymer Science and Technology in China)
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