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Polymers, Volume 18, Issue 12 (June-2 2026) – 141 articles

Cover Story (view full-size image): Ultra-high-molecular-weight polyethylene (UHMWPE) is the benchmark polymer for orthopedic hip and knee implants, prized for its highly linear, defect-free chain structure. This linearity has long made it seem unsuitable for thermal fractionation techniques that probe structural irregularities. This study shows otherwise: Successive Self-Nucleation and Annealing (SSA) successfully reveals hidden crystal populations within medical-grade UHMWPE, generated by entanglements introduced during processing. Combining SSA with micro-FTIR and cross-link analysis, the authors demonstrate how gamma irradiation, thermal stabilization, and oxidation reshape the crystalline architecture of conventional, highly cross-linked, and vitamin E-stabilized formulations, establishing SSA as a sensitive new tool for biomedical UHMWPE characterization. View this paper
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15 pages, 7015 KB  
Article
Influence of Self-Adhesive Resin Composite Deep Marginal Elevation on the Sealing Ability of CAD/CAM Lithium Disilicate Glass-Ceramic Inlays: An In Vitro Study
by Rasha Haridy, Shadan Almotairi, Shoroug Alshehri, Abrar Nasser Bin Nooh and Moataz Elgezawi
Polymers 2026, 18(12), 1555; https://doi.org/10.3390/polym18121555 - 22 Jun 2026
Viewed by 582
Abstract
Deep margin elevation (DME) is a conservative technique used to relocate subgingival proximal margins to a more favorable supragingival position, facilitating adhesive procedures and impression taking. This in vitro study evaluated the influence of two DME materials—a universal flowable resin composite and a [...] Read more.
Deep margin elevation (DME) is a conservative technique used to relocate subgingival proximal margins to a more favorable supragingival position, facilitating adhesive procedures and impression taking. This in vitro study evaluated the influence of two DME materials—a universal flowable resin composite and a self-adhesive flowable resin composite—on the cervical interfacial sealing ability of lithium disilicate glass–ceramic CAD/CAM inlay restorations. Twenty extracted maxillary premolars were randomly allocated into two groups (n = 10). Group A received DME using a universal flowable resin composite (3M™ Filtek™ Z350 XT) preceded by a conventional adhesive system, while Group B received DME using a self-adhesive flowable resin composite (Vertise™ Flow). All teeth were restored with lithium disilicate CAD/CAM inlays (CEREC Tessera) cemented with a self-adhesive resin cement (Breeze®). Specimens underwent thermocycling (10,000 cycles; 5–55 °C). Marginal gaps were assessed at the DME interface using high-resolution micro-computed tomography (micro-CT) in both coronal and sagittal cross-sections, before and after thermocycling. Statistically significant differences were found between groups in both sections before and after thermocycling (p < 0.05). The self-adhesive composite (Group B) demonstrated significantly lower gap values compared to the universal flowable composite (Group A) in both coronal and sagittal assessments. Thermocycling increased the gap in both groups; however, Group B maintained considerably lower leakage. The self-adhesive resin composite showed superior sealing ability at the DME interface compared to the universal flowable composite when used under lithium disilicate glass–ceramic inlay restorations. Further clinical studies are recommended to validate these findings. Full article
(This article belongs to the Special Issue Bio-Based Polymeric Materials for Biomedical Applications)
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16 pages, 1271 KB  
Article
Modulating Exciton Dynamics Through Fluorescent Side Group Incorporation in Benzodithiophene-Benzotriazole-Isoindigo Terpolymers
by René Hauyón, Yasmín Pérez, Daniela Zúñiga, Scarlet Araya, Bastian Camacho, Pablo Thomas, Cesar Saldías, Denis Fuentealba, Claudio A. Terraza, Felipe A. Angel and Ignacio A. Jessop
Polymers 2026, 18(12), 1554; https://doi.org/10.3390/polym18121554 - 22 Jun 2026
Viewed by 432
Abstract
In this work, we investigated the incorporation of a fluorescent side group, fluorescein octyl ester (FOE), in benzodithiophene-based donor–acceptor terpolymers as a strategy to modulate excited-state behavior. Three FOE-containing terpolymers (P2-iIa-c), obtained at different polymerization times, were systematically evaluated against an [...] Read more.
In this work, we investigated the incorporation of a fluorescent side group, fluorescein octyl ester (FOE), in benzodithiophene-based donor–acceptor terpolymers as a strategy to modulate excited-state behavior. Three FOE-containing terpolymers (P2-iIa-c), obtained at different polymerization times, were systematically evaluated against an analogous material without the fluorescent pendant unit (P1-iI). Thermal analysis revealed good thermal stability and an increase in glass transition temperature upon FOE incorporation, suggesting restricted segmental mobility and increased conformational constraints within the conjugated backbone. Optical characterization showed distinct absorption spectra with reaction time and shorter fluorescence lifetimes for the FOE-containing materials, consistent with the presence of additional excited-state deactivation pathways and intramolecular energy transfer processes within the terpolymer backbone. An approximate estimation of energy transfer efficiencies (≈60–65%) suggested that such processes may be operative within the system. Cyclic voltammetry measurements showed only minor variations in HOMO and LUMO energy levels between P1-iI and P2-iIa-c series, indicating that the conjugated backbone predominantly determined the frontier orbital energies despite side chain modification. Furthermore, photocurrent measurements from the bilayer device configuration exhibited a systematic increase in photocurrent for the FOE-containing material, supporting the role of excitonic modulation, rather than significant changes in interfacial energetic alignment. These results suggest that fluorescent side chain incorporation provides an effective strategy for regulating exciton dynamics while maintaining the electronic structure of the donor–acceptor terpolymer. Full article
(This article belongs to the Section Polymer Chemistry)
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25 pages, 6800 KB  
Article
PLA/PBSA Biocomposites Reinforced with Tangerine Tree-Derived Agro-Industrial Waste for Rigid Packaging: Effect of Extraction Treatment on Morphology and Thermo-Mechanical Performance
by Francesca Cartoni, Viola Berrugi, Aouatif Aboudia, Morad Chadni, Vito Gigante and Maria-Beatrice Coltelli
Polymers 2026, 18(12), 1553; https://doi.org/10.3390/polym18121553 - 22 Jun 2026
Viewed by 549
Abstract
Bio-based and biodegradable polymer composites based on polylactic acid (PLA) and polybutylene succinate-co-adipate (PBSA) were developed for rigid food packaging applications. Agro-industrial residues consisting of ground leaves and branches derived from tangerine tree cultivation (pruning) were used as fillers at high loading (30 [...] Read more.
Bio-based and biodegradable polymer composites based on polylactic acid (PLA) and polybutylene succinate-co-adipate (PBSA) were developed for rigid food packaging applications. Agro-industrial residues consisting of ground leaves and branches derived from tangerine tree cultivation (pruning) were used as fillers at high loading (30 wt%) before (PRE) or after (POST) extraction of bioactive compounds. The influence of blend composition (PLA/PBSA 60/40 and 30/70), filler extraction, and the addition of antioxidants (0.5 wt%) on material properties was systematically investigated. Composites were processed via extrusion and injection molding and characterized through FTIR, SEM, tensile testing and thermal analysis. The results show that polymer blend morphology affects mechanical behavior, with co-continuous structures (60/40) exhibiting improved ductility compared to dispersed systems (30/70). The incorporation of lignocellulosic residues increased stiffness but reduced elongation at break. Extraction treatment significantly modified filler morphology and interfacial interactions, slightly improving dispersion and processability. The effect of the extracted bioactive compounds on the thermal stabilization of biocomposites was also investigated. Overall, the findings demonstrate the potential of combining biodegradable polymer blends with treated agricultural residues to produce sustainable rigid packaging materials while supporting a bio-circular approach. In fact, preliminary extraction of valuable compounds from tangerine pruning waste appears to be a convenient strategy for its efficient cascade valorization. Full article
(This article belongs to the Section Biobased and Biodegradable Polymers)
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22 pages, 2484 KB  
Article
Synergistic Coatings Based on Chitosan and Eugenia caryophyllata Essential Oil to Improve Postharvest Quality of Capsicum chinense
by Fanor David Reyes Pérez, Yeimmy Peralta-Ruiz, Domingo César Carrascal-Hernández, Johannes Delgado-Ospina, Clemencia Chaves-López and Carlos David Grande-Tovar
Polymers 2026, 18(12), 1552; https://doi.org/10.3390/polym18121552 - 22 Jun 2026
Viewed by 472
Abstract
The topito pepper (Capsicum chinense) is a tropical fruit of economic and gastronomic importance in the Caribbean region, valued for its nutritional content. However, this fruit is susceptible to postharvest fungal diseases, including those caused by the phytopathogenic fungus Penicillium expansum [...] Read more.
The topito pepper (Capsicum chinense) is a tropical fruit of economic and gastronomic importance in the Caribbean region, valued for its nutritional content. However, this fruit is susceptible to postharvest fungal diseases, including those caused by the phytopathogenic fungus Penicillium expansum, which can degrade fruit quality and pose a health risk due to the potential presence of mycotoxins such as patulin. In this context, we evaluated the protective effects of coatings with chitosan (CS), clove essential oil (CEO), and their combination (CS+CEO) on sweet peppers stored at 12 °C for 12 days after harvest. The results indicate that the film-forming solution exhibited an acidic pH (5.33–5.44), a density of ~1.0 g/cm3, and viscosities ranging from 2.75 to 32.9 cP. Furthermore, the results indicate that coatings with CS and CS+CEO significantly reduced weight loss, preserved firmness (19.12–30.40 N), and delayed ripening. At the same time, the coatings exhibited inhibitory effects on P. expansum and aerobic mesophiles. The CS+CEO combination demonstrated the greatest inhibitory effect, indicating that it is a sustainable and effective strategy for the postharvest preservation of sweet peppers, thereby enhancing their value, preservation, and food security in the Caribbean region. Full article
(This article belongs to the Section Biobased and Biodegradable Polymers)
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17 pages, 1395 KB  
Article
Bioethanol from Miscanthus × giganteus: A Comparative Study of Different Pretreatment Technologies
by Ekaterina A. Skiba, Ekaterina I. Kashcheyeva, Vladimir N. Zolotukhin, Galina F. Mironova and Vera V. Budaeva
Polymers 2026, 18(12), 1551; https://doi.org/10.3390/polym18121551 - 22 Jun 2026
Viewed by 551
Abstract
Second-generation bioethanol technology is based on renewable raw materials with an unlimited potential for replenishment. However, the production cost of second-generation bioethanol is still higher than that of the first-generation. Biomass pretreatment is a key challenge, and solving it will improve the technology [...] Read more.
Second-generation bioethanol technology is based on renewable raw materials with an unlimited potential for replenishment. However, the production cost of second-generation bioethanol is still higher than that of the first-generation. Biomass pretreatment is a key challenge, and solving it will improve the technology efficiency. In this study, Miscanthus × giganteus from the Russian breeding stock was subjected to pretreatments with dilute HNO3 under atmospheric pressure. Pretreatments were carried out either as a single stage (HNO3) or as two stages ((i) HNO3 followed by NaOH, and (ii) NaOH followed by HNO3). Classical delignification with NaOH was also performed for comparison. Simultaneous saccharification and fermentation with delayed inoculation (dSSF) was then performed under identical conditions, with Saccharomyces cerevisiae Y-3136 as the microbial producer. Two-stage pretreatments were found to excel in purity, pulp composition, pulp conversion, bioethanol yield during fermentation, and raw bioethanol purity (impurities decreased by a factor of 21 compared to NaOH delignification). However, fermentation indicators are not the only critical aspect in bioethanol production technology. The complete cycle from Miscanthus × giganteus feedstock to the target bioethanol product was evaluated. The single-stage pretreatment with HNO3 performed best among the tested conditions. The HNO3 pretreatment achieved a 50% yield of pulps and a maximal bioethanol yield of 267 L/t, which is 44% higher compared to NaOH delignification. Furthermore, the HNO3 pretreatment enables savings in resources and electric power, as well as full commercial utilization of all polymers of the lignocellulosic matrix of the feedstock. Full article
(This article belongs to the Special Issue Advances in Lignocellulose: Cellulose, Hemicellulose and Lignin)
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24 pages, 3593 KB  
Article
Mulch Films Manufactured from Poly(Butylene Adipate-Co-Terephthalate) and Biopolymers Obtained from Urban and Agriculture Wastes: Mechanical Properties and Effects in Agriculture
by Enzo Montoneri, Philippe Evon, Jordane Charbonnier, Emanuele La Bella, Ferdinando Fragalà, Ivana Puglisi, Andrea Baglieri, Laurent Labonne, Landry Jégat, Solal Mendez, Simone Solaro, Elio Padoan and Jose L. Diéguez
Polymers 2026, 18(12), 1550; https://doi.org/10.3390/polym18121550 - 22 Jun 2026
Viewed by 724
Abstract
Biopolymers (BPs), obtained from urban and agricultural wastes, are known as active principles to manufacture ready-for-use finished products in several sectors of the agriculture and chemical industries. These findings prospect a biowaste-based refinery producing chemical specialities to replace products derived from fossil feedstock. [...] Read more.
Biopolymers (BPs), obtained from urban and agricultural wastes, are known as active principles to manufacture ready-for-use finished products in several sectors of the agriculture and chemical industries. These findings prospect a biowaste-based refinery producing chemical specialities to replace products derived from fossil feedstock. The present paper reports new materials containing BPs. Composite granules containing Poly(Butylene Adipate-Co-Terephthalate (PBAT) as a matrix and BPs as fillers are manufactured by twin-screw extrusion. The granules are used to make single-layer PBAT-BP mulch films by single-screw extrusion and three-layer Starch-PBAT-BP films by blown co-extrusion. The films are tested for mechanical properties, and for structural stability and effects in the in vitro cress germination and the in-field horticulture. The results show that both the films’ effects on plant performance and the films’ structural degradation are regulated by the BP and polymeric matrix release kinetics in the operational germination medium or the field soil, and in turn, that the kinetics depend on the mulch film structural features. The horticulture trials prove that the three-layer mulch films have adequate mechanical strength (25 MPa maximum tensile strength and 520% elongation at break) and about 6 months lifespan to maintain and/or improve the soil protection and crop production (17 t/ha) over the plant seasonal cycle. These findings widen the range of renewable chemical specialities potentially producible by the envisioned biowaste-based refinery. Full article
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13 pages, 2047 KB  
Article
Mechanical Properties of PUR and Latex Foams as Predictors for Seating or Lying Comfort
by Zoran Vlaović, Danijela Domljan, Tomislav Gržan and Goran Mihulja
Polymers 2026, 18(12), 1549; https://doi.org/10.3390/polym18121549 - 22 Jun 2026
Viewed by 520
Abstract
Flexible polyurethane (PUR) foams and latex rubber foams are widely used in furniture and mattress cushioning, yet conventional standardized mechanical tests only partially capture comfort-relevant behavior, particularly in layered constructions where material interactions and sequencing can alter elastic response. This study aimed to [...] Read more.
Flexible polyurethane (PUR) foams and latex rubber foams are widely used in furniture and mattress cushioning, yet conventional standardized mechanical tests only partially capture comfort-relevant behavior, particularly in layered constructions where material interactions and sequencing can alter elastic response. This study aimed to compare the mechanical (elastic) properties of selected three-layer composites of approximately 60 mm thickness (composed of conventional PUR, high-resilience PUR, low-resilience PUR, and latex foam) and to preliminarily assess whether combining foam types improves support of such setup and whether changing layer order modifies elasticity and support. Indentation hardness testing of multilayer cushions was conducted by ISO 2439:2008 Method E. Six three-layer systems (Alpha–Zeta) were assembled in two groups. Group X showed nearly identical support factors (2.6–2.7), high recovery (64.3–66.2%), low hysteresis loss (24.3–24.5%), and overlapping force–indentation (IFD) curves, indicating minimal effect of layer order and dominance of the PUR layers. Group Y exhibited higher but more sequence-dependent support (3.1–3.7), markedly reduced, wider range recovery (30.0–45.9%), increased hysteresis (33.0–34.7%), and more dispersed IFD curves. Placing high-resilience foam at the top partially improve recovery, whereas locating low-resilience foam at the surface increase energy loss. The research contributes in part to the body of knowledge about the behavior of the tested materials according to standardized rules. These preliminary results can be compared with other research findings and used in the preparation of testing models for multilayer foam composites, thereby generating new knowledge to improve the design of future experiments, which will result in increased sitting and lying comfort. Full article
(This article belongs to the Special Issue Advanced Polymer Composites and Foams)
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24 pages, 22612 KB  
Article
Effect of Beverages on the Surface Roughness and Staining of Modified Polyetheretherketone (PEEK) Materials
by Aybike Cengiz Dağtekin and Samet Tekin
Polymers 2026, 18(12), 1548; https://doi.org/10.3390/polym18121548 - 22 Jun 2026
Viewed by 478
Abstract
This study investigates color and surface alterations in neat and modified PEEK materials (10 × 3 mm, n = 140) immersed in various beverage solutions. Surface roughness (Ra) and color change (ΔE) were analyzed, supported by SEM and AFM evaluations. Specimens polished with [...] Read more.
This study investigates color and surface alterations in neat and modified PEEK materials (10 × 3 mm, n = 140) immersed in various beverage solutions. Surface roughness (Ra) and color change (ΔE) were analyzed, supported by SEM and AFM evaluations. Specimens polished with 400–1200 grit sandpaper were measured via profilometry before a 30-day immersion in distilled water, coffee, tea, cola, and red wine (refreshed every 12 h). Post-immersion results indicated that material and solution types significantly influenced Ra and ΔE values (p < 0.05), with the TP group being the least affected. Statistically, tea caused the greatest discoloration. The GFP group exhibited the highest Ra, indicating inferior surface stability, whereas TP and CR groups remained below the 0.2 μm clinical threshold. Specifically, the TP group demonstrated the lowest Ra value. Although perceptible color changes occurred in all materials, a positive correlation was identified between material type and beverage solutions. SEM and AFM analyses confirmed the presence of surface micro-cracks and morphological irregularities. Full article
(This article belongs to the Special Issue Surface and Interface Analysis of Polymeric Materials)
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18 pages, 7233 KB  
Article
Electrospinning of Polycaprolactone Membranes Using Green Solvents for Organ-on-a-Chip Applications
by Donna Danijela Dragun, Karla Kuzman, Marta Blažek, Petra Popović, Floren Radovanović-Perić, Iva Rezić Meštrović, Fabio Faraguna and Ernest Meštrović
Polymers 2026, 18(12), 1547; https://doi.org/10.3390/polym18121547 - 22 Jun 2026
Viewed by 634
Abstract
Electrospinning is a highly versatile technique for fabricating nanofibrous membranes with high surface-area-to-volume ratios and tunable porosity. Although polycaprolactone (PCL) is widely utilized in biomedical engineering due to its biocompatibility, its electrospinning traditionally relies on hazardous organic solvents like dichloromethane (DCM) and N,N-dimethylformamide [...] Read more.
Electrospinning is a highly versatile technique for fabricating nanofibrous membranes with high surface-area-to-volume ratios and tunable porosity. Although polycaprolactone (PCL) is widely utilized in biomedical engineering due to its biocompatibility, its electrospinning traditionally relies on hazardous organic solvents like dichloromethane (DCM) and N,N-dimethylformamide (DMF). This paper details the development of a fully sustainable, green electrospinning process for PCL using a bio-derived binary mixture of acetic acid and formic acid. Processing parameters (applied voltage, tip-to-collector distance, and flow rate) were systematically optimized using a Design of Experiments (DoE) response surface methodology. Scanning electron microscopy (SEM) confirmed the successful fabrication of uniform, bead-free nanofibers with a mean diameter of 247 nm, representing a 37.3% reduction compared to conventional DCM:DMF-spun matrices. Fourier-transform infrared spectroscopy (FTIR) verified complete solvent evaporates. Full article
(This article belongs to the Section Circular and Green Sustainable Polymer Science)
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14 pages, 1309 KB  
Article
Effect of Fiber and Metal Reinforcement on the Flexural Properties of Printed and Conventional Provisional Restorative Materials
by João Carlos Ramos, Gabriela Almeida, Francisco Silva, Neila Gani, Ana Messias and Alexandra Vinagre
Polymers 2026, 18(12), 1546; https://doi.org/10.3390/polym18121546 - 22 Jun 2026
Viewed by 457
Abstract
(1) Background: Provisional restorations play a crucial role in maintaining oral function and must exhibit adequate mechanical properties, particularly fracture resistance, to ensure structural integrity throughout the provisional phase. The aim of this study was to compare the flexural strength and modulus of [...] Read more.
(1) Background: Provisional restorations play a crucial role in maintaining oral function and must exhibit adequate mechanical properties, particularly fracture resistance, to ensure structural integrity throughout the provisional phase. The aim of this study was to compare the flexural strength and modulus of materials used for provisional dental prostheses, with and without fiber or metal reinforcement. (2) Methods: Standardized specimens (2 × 2 × 25 mm) were fabricated from an acrylic resin (Unifast LC), a 3D-printed resin (NextDent C&B), and a bis-acryl resin (Luxatemp Fluorescence). For each material, four experimental subgroups were established: no reinforcement, two types of glass fiber reinforcement (EverStick C&B and EverStick Post NET), and metal reinforcement. Specimens were subjected to a three-point bending test. Flexural strength and flexural modulus were analyzed using a two-way, non-parametric ANOVA with the aligned rank transform. The significance level was set at 0.05. (3) Results: Material type and reinforcement strategy significantly affected flexural strength and flexural modulus. Fiber reinforcement with EverStick C&B yielded the highest values across all materials, particularly in the acrylic resin. Metal reinforcement showed moderate improvements, whereas EverStick NET had limited or no effect and reduced strength in the bis-acryl resin. Reinforced specimens exhibited altered fracture behavior, preventing complete separation after failure. (4) Conclusions: Fiber reinforcement, particularly with EverStick C&B, significantly enhances the flexural strength and modulus of provisional materials. The reinforcement performance is dependent on its type and material interaction, modifying fracture behavior by preventing complete separation. Full article
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17 pages, 1484 KB  
Article
Assessment of Surface Roughness and Bacterial Adhesion of Occlusal Splints Fabricated with Different Layer Thicknesses, Polishing Techniques and Build Orientations
by Merve Dede, Sina Saygili and Nursen Topcuoglu
Polymers 2026, 18(12), 1545; https://doi.org/10.3390/polym18121545 - 22 Jun 2026
Viewed by 1456
Abstract
This study evaluated the combined effects of build orientation, layer thickness, and polishing protocols on surface roughness and bacterial adhesion of occlusal splints. Ten disc-shaped specimens (Ø16 × 3 mm) were fabricated for each group using a digital light processing (DLP)-based 3D printer. [...] Read more.
This study evaluated the combined effects of build orientation, layer thickness, and polishing protocols on surface roughness and bacterial adhesion of occlusal splints. Ten disc-shaped specimens (Ø16 × 3 mm) were fabricated for each group using a digital light processing (DLP)-based 3D printer. Specimens were printed at two orientations (0° and 90°) and two layer thicknesses (50 and 100 µm) using a splint resin. Surface roughness was measured with a contact profilometer, and bacterial adhesion was measured by optical density (OD) readouts for Streptococcus mutans using a spectrophotometer. Surface morphology was examined by field-emission scanning electron microscopy (SEM). Statistical analyses were performed using jamovi. Because normality and/or homogeneity assumptions were not met, robust analysis of variance was applied. Polishing protocol significantly affected surface roughness (Ra) values. Unpolished specimens showed the highest Ra values, whereas mechanical polishing combined with centrifugation produced the lowest values. No significant main effects of polishing protocol, layer thickness or orientation were observed for bacterial adhesion. SEM findings supported the roughness results. Surface roughness was primarily influenced by polishing protocols and their interactions, whereas bacterial adhesion remained relatively stable. The weak Ra–OD correlation indicated that surface roughness alone was not a reliable predictor of bacterial adhesion. Full article
(This article belongs to the Special Issue Advanced Polymers for Dental Applications)
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18 pages, 16509 KB  
Article
Influence of PLA Flowability and Talc Content on the Performance of Rigid TPS/PBS/PLA/Talc Blends
by Cristina Martín-Poyo, Josep P. Cerisuelo and Jose D. Badia-Valiente
Polymers 2026, 18(12), 1544; https://doi.org/10.3390/polym18121544 - 21 Jun 2026
Viewed by 535
Abstract
This study investigates the influence of PLA flowability and talc content on the performance of compostable thermoplastic starch/poly(butylene succinate) (TPS/PBS)-based systems for rigid applications. Different PLA grades with varying melt flow index (PLA23, PLA8 and PLA70) and talc contents (0, 5 and 10 [...] Read more.
This study investigates the influence of PLA flowability and talc content on the performance of compostable thermoplastic starch/poly(butylene succinate) (TPS/PBS)-based systems for rigid applications. Different PLA grades with varying melt flow index (PLA23, PLA8 and PLA70) and talc contents (0, 5 and 10 wt%) were incorporated. Twelve formulations were compounded by twin-screw extrusion and processed by injection moulding. FTIR confirmed the coexistence of TPS, PBS and PLA phases without evidence of chemical interactions. Morphological analysis showed that PLA flowability plays a key role in phase distribution, with higher-flow PLA promoting improved dispersion and interfacial adhesion, while talc addition (5 and 10 wt%) increased structural heterogeneity; at higher loadings, particularly, DSC analysis revealed that talc acted as a nucleating agent for the PBS phase, increasing crystallisation temperatures from approximately 73 °C to 81 °C depending on formulation. Mechanical results showed that Young’s modulus increased from approximately 1.4 GPa to 2.7 GPa with decreasing PLA flowability and increasing talc content. Formulations containing low-flow PLA reached tensile strengths close to 32 MPa, although elongation at break decreased to values near 2%. In contrast, high-flow PLA formulations exhibited a more balanced mechanical response, with elongation values up to approximately 8%, associated with improved phase dispersion. Hybrid PLA systems showed intermediate behaviour, reaching elongations up to 22% while maintaining modulus values around 1.8 GPa. Talc provided additional reinforcement but reduced deformation capacity. HDT values remained relatively constant, indicating limited improvement in thermomechanical resistance despite increased stiffness. These results demonstrate that the combined control of PLA molecular characteristics and talc content enables tuning of the mechanical and thermomechanical performance of TPS/PBS/PLA/talc systems for rigid packaging applications. Full article
(This article belongs to the Special Issue Design and Performance of Compostable Polymeric Packaging Materials)
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26 pages, 11921 KB  
Article
Comparative Evaluation of β-TCP-Based Composite Biomaterials Using Chorionic Mesenchymal Stem Cells Under Non-Osteogenic Conditions
by Jana Čajková, Marianna Trebuňová, Darina Bačenková, Gabriela Ižaríková, Erik Dosedla and Jozef Živčák
Polymers 2026, 18(12), 1543; https://doi.org/10.3390/polym18121543 - 21 Jun 2026
Viewed by 575
Abstract
This study evaluates the intrinsic osteogenic potential of β-tricalcium phosphate (β-TCP)-containing composite scaffolds (PLCL–TCP, PLGA–TCP, and ZnO–TCP) on chorion-derived mesenchymal stem cells (CMSCs) under non-osteogenic in vitro conditions. CMSCs were cultured on the three biomaterials for 35 days without osteogenic supplements to isolate [...] Read more.
This study evaluates the intrinsic osteogenic potential of β-tricalcium phosphate (β-TCP)-containing composite scaffolds (PLCL–TCP, PLGA–TCP, and ZnO–TCP) on chorion-derived mesenchymal stem cells (CMSCs) under non-osteogenic in vitro conditions. CMSCs were cultured on the three biomaterials for 35 days without osteogenic supplements to isolate the material-driven cellular response. Cell viability was assessed via MTT assay, while osteogenesis-associated markers (alkaline phosphatase, type I collagen, and osteocalcin) were quantified using ELISA. Scaffold surface morphology and elemental composition were characterized before and after cultivation utilizing SEM and EDX. All investigated scaffolds supported long-term CMSC viability and induced measurable osteogenic responses. PLCL–TCP demonstrated a consistently strong biological response, characterized by sustained metabolic activity, elevated ALP and COL I production, and increased osteocalcin levels at later stages of cultivation. ZnO–TCP also exhibited favorable osteogenesis-associated responses, particularly with respect to late-stage osteocalcin production, while maintaining high structural stability. In conclusion, β-TCP composites can intrinsically modulate CMSC behavior without biochemical supplements. Osteogenic outcomes depend on a complex interplay of surface chemistry, scaffold architecture, and degradation profiles, with PLCL–TCP demonstrating favorable overall performance among the investigated biomaterials. Full article
(This article belongs to the Special Issue Modification of Natural Biodegradable Polymers)
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21 pages, 2551 KB  
Article
Sulfonation-Time-Dependent Structure–Property Relationships of Electrospun Polyketone Nanofiber Membranes for PEMFC Applications
by Hongsik Byun, Geon-Hyeong Lee, Yeol-Lim Lee and Sang-Hun Lee
Polymers 2026, 18(12), 1542; https://doi.org/10.3390/polym18121542 - 21 Jun 2026
Viewed by 628
Abstract
Electrospun sulfonated polyketone (PK) nanofiber membranes were prepared to investigate the sulfonation-time-dependent structure–property relationships of hydrocarbon-based polymer electrolyte membranes for PEMFC (Polymer Electrolyte Membrane Fuel Cell) applications. NaCl addition to the electrospinning solution increased solution conductivity and enabled the formation of uniform PK [...] Read more.
Electrospun sulfonated polyketone (PK) nanofiber membranes were prepared to investigate the sulfonation-time-dependent structure–property relationships of hydrocarbon-based polymer electrolyte membranes for PEMFC (Polymer Electrolyte Membrane Fuel Cell) applications. NaCl addition to the electrospinning solution increased solution conductivity and enabled the formation of uniform PK nanofibers with an average diameter of approximately 270 nm. Subsequent sulfonation introduced sulfonic-acid-related groups into the PK nanofiber framework, and the resulting membrane properties were strongly governed by sulfonation time. Among the tested membranes, PK-NC16 exhibited the highest proton conductivity of 0.107 ± 0.031 S cm−1 and an ion exchange capacity of 2.82 meq g−1, exceeding or comparable to those of Nafion 115 under the tested conditions. FTIR-based analysis indicated that the relative sulfonation index increased up to 16 h, whereas extended sulfonation for 24 h generated additional sulfone/sulfonate-related bands, suggesting possible side reactions or structural changes under prolonged acid treatment. The high water uptake of PK-NC16 enhanced proton transport but also revealed a hydration-sensitive polymer network, as reflected by a voltage degradation rate of approximately −590 μV h−1 during a 100 h short-term stability constant-current test. These results demonstrate that sulfonation time is a key parameter controlling the balance among ionic functionality, hydration, mechanical response, proton conductivity, and PEMFC-relevant single-cell performance in electrospun PK nanofiber membranes. Full article
(This article belongs to the Special Issue Multifunctional Application of Electrospun Fiber: 2nd Edition)
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15 pages, 4106 KB  
Article
Eggshell Particle-Reinforced PVA/GO Hydrogel with Self-Healing Effect
by Banu Esencan Türkaslan and Merve Dogu
Polymers 2026, 18(12), 1541; https://doi.org/10.3390/polym18121541 - 21 Jun 2026
Viewed by 527
Abstract
Self-healing biomaterials have attracted significant attention due to their ability to restore structural integrity, extend material lifetime, and reduce maintenance costs without external intervention. In this study, Polyvinyl Alcohol/Graphene Oxide/Eggshell Particle (PVA/GO/ESP) composite hydrogels were synthesized via a freeze–thawing method and characterized using [...] Read more.
Self-healing biomaterials have attracted significant attention due to their ability to restore structural integrity, extend material lifetime, and reduce maintenance costs without external intervention. In this study, Polyvinyl Alcohol/Graphene Oxide/Eggshell Particle (PVA/GO/ESP) composite hydrogels were synthesized via a freeze–thawing method and characterized using XRD, SEM/EDS, and FTIR analyses. The effect of ESP incorporation on the self-healing and mechanical properties of the hydrogels was systematically investigated. Tensile test results demonstrated that incorporation of 1 wt% ESP improved the tensile strength up to 0.326 MPa while maintaining high strain capacity. Healing efficiency values calculated from recovered tensile strength showed approximately 69%, 47%, and 67% recovery for PVA/GO, PVA/GO/ESP (0.5%), and PVA/GO/ESP (1%) hydrogels, respectively. The developed hydrogels demonstrated rapid self-healing behavior at room temperature without external stimuli. These findings suggest that ESP-reinforced PVA/GO hydrogels may serve as promising candidates for future biomaterial and soft tissue engineering studies. The developed hydrogels demonstrated enhanced tensile strength, rapid self-healing behavior, and promising swelling properties, indicating their potential use in soft tissue engineering and biomaterial applications. Full article
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19 pages, 2944 KB  
Article
Cell Structure Regulation of Polypropylene/Ethylene-Propylene Rubber Bead Foams and Enhanced Mechanical Properties of Their Molded Products
by Zi’ang Hu, Xiulu Gao, Yichong Chen, Jiacheng Wang, Ling Zhao and Dongdong Hu
Polymers 2026, 18(12), 1540; https://doi.org/10.3390/polym18121540 - 21 Jun 2026
Viewed by 526
Abstract
To improve the foamability and steam-chest molding performance of polypropylene (PP) bead foams, ethylene-propylene rubber (EPR) was introduced into PP via melt blending. The role of EPR in the complete bead-foaming-to-molding process was systematically investigated by correlating phase morphology, crystallization behavior, melt viscoelasticity, [...] Read more.
To improve the foamability and steam-chest molding performance of polypropylene (PP) bead foams, ethylene-propylene rubber (EPR) was introduced into PP via melt blending. The role of EPR in the complete bead-foaming-to-molding process was systematically investigated by correlating phase morphology, crystallization behavior, melt viscoelasticity, CO2 dissolution and diffusion, cellular structure, inter-bead welding, and the mechanical properties of molded foam products. The incorporation of EPR refined the PP crystalline morphology, reduced the apparent crystallinity, and markedly enhanced the melt viscoelasticity, thereby broadening the foaming temperature window. The dispersed EPR phase functioned simultaneously as a CO2 reservoir and a high-diffusivity pathway of CO2, which promoted cell growth while suppressing excessive nucleation. The enhanced melt viscoelasticity and improved CO2 affinity promoted bead expansion and optimized the cellular structure. At 150 °C, the expansion ratio increased from 18.7 for neat PP to 21.1 with 10 wt% EPR. EPR also regulated the cellular structure. At 150 °C, the cell diameter increased from 83 to 176 μm as the EPR content increased from 0 to 20 wt%. EPR markedly changed the double-melting behavior of PP bead foams. The low-temperature melting enthalpy increased from 28.5 J/g for neat PP to 37.8 J/g with 10 wt% EPR, which served as an effective interfacial binder, significantly promoting inter-bead welding. Consequently, the optimized PP/EPR foam containing 10 wt% EPR exhibited a tensile strength of 1.13 MPa and an elongation at break of 22.1%. More importantly, excellent molding quality was achieved at a reduced steam pressure of 2.2 bar, demonstrating the great potential of PP/EPR bead foams for the energy-efficient manufacturing of high-performance lightweight products. Full article
(This article belongs to the Special Issue Advances in Thermoplastic Polymer Composites)
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22 pages, 2093 KB  
Review
Polymer-Based Coatings for Cardiovascular and Endovascular Devices: Linking Surface Chemistry, Drug Release Kinetics, and Thrombo-Inflammatory Performance: A Review
by Rasit Dinc and Nurittin Ardic
Polymers 2026, 18(12), 1539; https://doi.org/10.3390/polym18121539 - 20 Jun 2026
Viewed by 720
Abstract
Polymer coatings are integral to nearly every modern cardiovascular and endovascular device, including drug-eluting stents (DESs) and drug-coated balloons (DCBs), bioabsorbable vascular scaffolds (BVSs), occluders, grafts, and catheter and guidewire hydrophilic surfaces. Persistent complications, including late stent thrombosis, delayed endothelialization, hypersensitivity, and restenosis, [...] Read more.
Polymer coatings are integral to nearly every modern cardiovascular and endovascular device, including drug-eluting stents (DESs) and drug-coated balloons (DCBs), bioabsorbable vascular scaffolds (BVSs), occluders, grafts, and catheter and guidewire hydrophilic surfaces. Persistent complications, including late stent thrombosis, delayed endothelialization, hypersensitivity, and restenosis, show that coatings actively shape biological responses rather than acting as inert drug carriers. Their surface chemistry, drug release kinetics, and degradation behavior are upstream determinants of blood– and tissue–material responses that govern healing and failure. This review frames coating selection as a structure–property–biological response problem. It surveys the major classes of synthetic polymer coatings and the defining surface and bulk properties. This review also examines how composition and architecture control drug release, and traces the interfacial cascade of protein adsorption, coagulation and complement activation, platelet and leukocyte responses, and neutrophil extracellular trap (NET) formation. These mechanisms are linked to contemporary design strategies that improve hemocompatibility, limit thrombosis, promote endothelial recovery, and tune degradation, and to the standardization and translation gaps that remain. The central message is that polymer coatings are not biologically equivalent. Their surface chemistries and degradation profiles determine the thrombo-inflammatory outcomes. Therefore, coating design should be guided by intended biological response, not drug release alone. Full article
(This article belongs to the Special Issue Polymer-Based Coatings: Principles, Development and Applications)
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31 pages, 20808 KB  
Article
Fracture Mode Transition and Energy Dissipation of Brittle Coal Under Confinement Induced by a Flexible Polyurea Coating
by Shan Ning, Weibing Zhu, Biao Fu, Pengjun Gao and Zishuo Jia
Polymers 2026, 18(12), 1538; https://doi.org/10.3390/polym18121538 - 20 Jun 2026
Viewed by 454
Abstract
Brittle geomaterials such as coal and rock are prone to unstable failure under high stress and dynamic disturbances, where rapid release of stored elastic strain energy can trigger dynamic disasters. Polyurea, a high-strength and high-ductility elastomer, can form a continuous flexible coating on [...] Read more.
Brittle geomaterials such as coal and rock are prone to unstable failure under high stress and dynamic disturbances, where rapid release of stored elastic strain energy can trigger dynamic disasters. Polyurea, a high-strength and high-ductility elastomer, can form a continuous flexible coating on the surface of coal/rock to regulate their deformation–fracture behavior. Here, uniaxial compression tests were performed on coal specimens coated with polyurea layers of different thicknesses (0–1.25 mm). Acoustic emission (AE) and digital image correlation (DIC) were jointly employed to characterize macroscopic deformation, microcrack evolution, fracture-mode transition, and energy partitioning. The results show that polyurea provides passive lateral confinement that suppresses lateral expansion and shifts macroscopic failure from brittle splitting to progressive ductile damage. AE-based AF–RA analysis indicates that thicker coatings increase the normal stress and shear resistance along potential fracture planes, promoting a microfracture transition from shear-dominated to tension-dominated cracking. Energy analysis demonstrates that the coating enhances pre-peak energy dissipation via coordinated deformation with the coal, while thicker coatings (≥1.00 mm) exhibit pronounced post-peak elastic tensile deformation to absorb and buffer fracture-released energy, impeding the instantaneous energy release typical of bare coal. Moreover, the elastic energy index shows that polyurea markedly reduces impact tendency, with an appropriate thickness stabilizing specimens from strong to weak/non-impact propensity. These findings clarify the coupled confinement–fracture–energy regulation mechanisms of polyurea coatings and provide quantitative guidance for coating-thickness design to mitigate dynamic failure hazards in brittle materials. Full article
(This article belongs to the Section Polymer Networks and Gels)
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23 pages, 2051 KB  
Article
Lyophilized Chitosan-Based Hydrogels as a Potential Stimuli-Responsive Carrier System for Anti-Inflammatory Drugs: Ibuprofen Solubility Modulation at Variable pH of Simulated GIT Conditions
by Veronika Mikušová, Jarmila Prieložná, Dominika Žigrayová, Michal Hanko and Peter Mikuš
Polymers 2026, 18(12), 1537; https://doi.org/10.3390/polym18121537 - 20 Jun 2026
Viewed by 493
Abstract
Poor aqueous solubility and consequently low bioavailability of various NSAIDs (non-steroidal anti-inflammatory drugs) usually result in high and multiple dosing with potentially serious side effects. Therefore, systems for the effective transport of NSAIDs through the GIT (gastrointestinal tract), ensuring enhanced bioavailability, remain in [...] Read more.
Poor aqueous solubility and consequently low bioavailability of various NSAIDs (non-steroidal anti-inflammatory drugs) usually result in high and multiple dosing with potentially serious side effects. Therefore, systems for the effective transport of NSAIDs through the GIT (gastrointestinal tract), ensuring enhanced bioavailability, remain in high demand. In the present work, we studied chitosan (CS) hydrogel lyophilizates as carrier systems for a model NSAID, namely ibuprofen (IBU). The CS-IBU lyophilizates were prepared from homogeneous or heterogeneous CS-IBU hydrogels to assess their influence on the resulting lyophilizate microstructure and IBU dissolution profiles. To gain a complex view of the CS-IBU behavior and its practical consequences, dissolution profiles of free IBU (reference) and CS-associated IBU (CS-IBU) were examined and compared to each other at variable pH (1.2 and 6.5) in two separate dissolution systems and in one discontinuous dissolution system mimicking GIT conditions. The results of dissolution experiments were supported by kinetic model data. This study demonstrated that the dissolution of IBU from the CS-IBU lyophilizates is affected by two main pH-dependent competitive effects; i.e., dissolved CS acts as an IBU solubilizer and the undissolved CS matrix serves as an IBU trap, which could be used in the rational design of innovative stimuli (pH)-responsive oral dosage forms of IBU. Full article
(This article belongs to the Special Issue Bio-Based Polymeric Materials for Biomedical Applications)
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18 pages, 2807 KB  
Article
Fully Aqueous Electrospinning of Binary PVP/Sodium-Alginate and PVP/Riboflavin Nanofibres: Additive Effects and UV-Assisted Processing
by Julia C. Andrade, Gilmar P. Thim, Fernando Cabral, Frank Jorg Clemens and Marcio Fredel
Polymers 2026, 18(12), 1536; https://doi.org/10.3390/polym18121536 - 20 Jun 2026
Cited by 1 | Viewed by 560
Abstract
Electrospinning (ES) can produce nonwoven fibrous mats with high surface area and interconnected porosity, making them attractive for biomedical and functional material applications. However, conventional ES often relies on volatile organic solvents, raising safety, environmental, and translational concerns. Fully aqueous (“green”) ES offers [...] Read more.
Electrospinning (ES) can produce nonwoven fibrous mats with high surface area and interconnected porosity, making them attractive for biomedical and functional material applications. However, conventional ES often relies on volatile organic solvents, raising safety, environmental, and translational concerns. Fully aqueous (“green”) ES offers an appealing alternative, although many water-soluble polymers remain difficult to spin and may show limited stability under hydrated conditions. In this study, two fully aqueous binary systems, poly(vinylpyrrolidone)–sodium alginate (PVP–SA) and poly(vinylpyrrolidone)–riboflavin (PVP–RF), were investigated to decouple the roles of sodium alginate (SA) and riboflavin (RF) on solution behaviour, fibre formation, morphology, dry-state mechanical properties, and surface chemistry. Aqueous PVP solutions (20% w/v; molecular weight 1.3 MDa) were blended with SA (1–5 wt% relative to PVP) or RF (1–10 wt% relative to PVP). Electrical conductivity and rheological properties were evaluated prior to ES under controlled conditions, with simultaneous ultraviolet (UV) exposure at 344 nm during fibre collection. RF did not significantly alter conductivity (~0.74–0.75 µS·cm−1), whereas SA increased conductivity up to 2.75 ± 0.03 µS·cm−1 at 5 wt%. All formulations exhibited shear-thinning behaviour, while 10 wt% RF increased the zero-shear viscosity relative to neat PVP. Morphological analysis showed that low SA contents produced uniform fibres, whereas higher SA levels (4–5 wt%) led to bead defects and reduced fibre diameter (down to 85 ± 25 nm). Dry-state mechanical performance decreased with increasing SA content, while 10 wt% RF improved tensile strength and toughness, reaching an ultimate tensile strength of 5.21 ± 0.15 MPa and toughness of 40.51 ± 1.53 MJ·m−3. Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) indicated subtle UV-driven redistribution of surface chemical states, consistent with mild photo-oxidative microstructural modification rather than extensive covalent network formation. Because the UV irradiance was not directly measured and wet-state stability was not assessed, the UV-related findings are interpreted as preliminary chemical evidence rather than confirmation of stabilized fibre mats. Overall, this work establishes a solvent-free aqueous ES platform in which ionic and photoactive additives can be used to tailor fibre morphology, dry-state mechanical behaviour, and surface characteristics without toxic reagents. Full article
(This article belongs to the Special Issue Advances in Electrospun Polymeric Nanofibers)
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22 pages, 4243 KB  
Article
Preparation of an MMT-Modified Hyperbranched Adsorbent and Its Application in the Selective Adsorption of Pb(II)
by Wei Gong, Shitong Xie, Meilan Li, Qiang Xie, Yinyin Zhou, Yutong Sun and Guochun Zhang
Polymers 2026, 18(12), 1535; https://doi.org/10.3390/polym18121535 - 20 Jun 2026
Viewed by 403
Abstract
The P(IA-HBP-AA-AM)/MMT composite was successfully synthesized via in situ polymerization and characterized using FTIR, XRD, TGA, and other techniques. The material was then applied as an adsorbent for the removal of heavy metals from simulated mining-contaminated water (prepared based on the typical ionic [...] Read more.
The P(IA-HBP-AA-AM)/MMT composite was successfully synthesized via in situ polymerization and characterized using FTIR, XRD, TGA, and other techniques. The material was then applied as an adsorbent for the removal of heavy metals from simulated mining-contaminated water (prepared based on the typical ionic composition of real mining wastewater). Static adsorption experiments revealed that P(IA-HBP-AA-AM)/MMT composite could efficiently remove Pb(II) from contaminated water, and the adsorption behavior was well described by the pseudo-second-order kinetic model and the Langmuir isotherm model. Thermodynamic analysis indicated that the adsorption of Pb(II) onto the P(IA-HBP-AA-AM)/MMT composite was an endothermic and spontaneous process. At pH = 4.5 and T = 45 °C, the maximum adsorption capacity obtained from model fitting was 249.38 mg/g. The material exhibited strong selectivity for Pb(II), even in the presence of competing metal ions such as Cd(II), Zn(II), Al(III), Fe(III), K(I), and Na(I). Moreover, after five adsorption–desorption cycles, it still retained approximately 90% of its Pb(II) removal efficiency. Furthermore, dynamic adsorption experiments showed that the saturation adsorption capacity of Pb(II) reached 178.7 mg/g, with a column utilization efficiency of approximately 41%. These findings demonstrate the promising potential of P(IA-HBP-AA-AM)/MMT composite for the removal of Pb(II) from mining-contaminated water. Full article
(This article belongs to the Collection Polymer Applications in Environmental Science)
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18 pages, 24432 KB  
Article
Degradable Polyurethane Foams Based on Amino Acid Phosphoramides (APtA)
by Nico Vennemann, Anton Bauer and Oliver Brüggemann
Polymers 2026, 18(12), 1534; https://doi.org/10.3390/polym18121534 - 20 Jun 2026
Viewed by 523
Abstract
Soft polyurethane foams are commonly found in furniture, mattresses, shoes and soundproofing applications. These crosslinked foams are hard to recycle. This paper describes our approach of introducing chemical breakage points based on amino acid phosphoramidates (APtA) in the PUs’ backbones. The APtA monomers [...] Read more.
Soft polyurethane foams are commonly found in furniture, mattresses, shoes and soundproofing applications. These crosslinked foams are hard to recycle. This paper describes our approach of introducing chemical breakage points based on amino acid phosphoramidates (APtA) in the PUs’ backbones. The APtA monomers are combined with PEG, PPG and pTHF-chains to achieve different monomer structures. We demonstrate the hydrolysis of these APtA monomers at neutral pH 7 and the mass loss of the foams. It is shown that after 70 days, more than 50% of the p-THF-APtA monomer and 35% of the PPG-APtA monomer have degraded. However, a contrary trend was observed for the foams, with only 2.5% mass loss for the p-THF-APtA foam, but 26% mass loss for the PPG-APtA foam. The foams were also characterized using compression measurements, revealing a stiffer appearance of the p-THF-APtA foam compared to the foams based on PEG and PPG. SEM images were taken before and after the degradation of the foams to show the difference in morphology. Full article
(This article belongs to the Section Circular and Green Sustainable Polymer Science)
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9 pages, 1807 KB  
Article
Laser-Induced Nanocarbon Films Enable Optical Sensor Based on Combined Photothermal and Piezoresistive Effect
by Yanbo Yao, Jingwen Yao and Tao Liu
Polymers 2026, 18(12), 1533; https://doi.org/10.3390/polym18121533 - 19 Jun 2026
Viewed by 480
Abstract
This work presents an enhanced photomechanical optical sensor inspired by our previously reported bio-inspired uncooled infrared detector. Performance improvement is achieved by strengthening the interfacial bond between the photothermal dendrite—polydopamine nanoparticle (PDA NP)/polydimethylsiloxane (PDMS) composite—and the piezoresistive laser-induced nanocarbon film, with a flexible [...] Read more.
This work presents an enhanced photomechanical optical sensor inspired by our previously reported bio-inspired uncooled infrared detector. Performance improvement is achieved by strengthening the interfacial bond between the photothermal dendrite—polydopamine nanoparticle (PDA NP)/polydimethylsiloxane (PDMS) composite—and the piezoresistive laser-induced nanocarbon film, with a flexible PDMS substrate that provides both thermal insulation and mechanical stability. The resulting sensor exhibits a responsivity of 51.6 W−1 under 808 nm irradiation, an order-of-magnitude enhancement over the unmodified device. Wavelength-dependent characterization (455–1550 nm) shows responsivity decreasing from 93.1 W−1 at 455 nm to 14.4 W−1 at 1550 nm, with response times on the order of seconds across this range. Extending this trend into the longer-wavelength region of blackbody radiation, the mechanism transitions to a predominantly bolometric mode. The device also demonstrates stable detection of several hundred microwatts and robust durability at 455 nm. These results validate interface engineering strategy as a viable pathway toward high-performance uncooled optical detection, advancing bio-inspired detectors from functional mimicry toward an application-ready platform. These findings confirm PDA NPs as effective photothermal converters primarily at shorter wavelengths, while the wavelength-dependent response suggests future tailoring of spectral sensitivity using long-wavelength-absorbing materials. Full article
(This article belongs to the Section Smart and Functional Polymers)
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28 pages, 26663 KB  
Article
Advanced Digital Imaging Assessment Method for Testing Surface Fuzzing in Textile Materials
by Juro Živičnjak, Antoneta Tomljenović, Maja Somogyi Škoc and Željko Penava
Polymers 2026, 18(12), 1532; https://doi.org/10.3390/polym18121532 - 19 Jun 2026
Viewed by 512
Abstract
Textile materials made from staple fibers typically have protruding fibers on their surface, commonly referred to as surface hairiness. During fraying, the surface of the textile material is susceptible to damage, which affects its appearance and leads to fuzzing by roughening or the [...] Read more.
Textile materials made from staple fibers typically have protruding fibers on their surface, commonly referred to as surface hairiness. During fraying, the surface of the textile material is susceptible to damage, which affects its appearance and leads to fuzzing by roughening or the emergence of new fibers. The propensity for fuzzing is assessed using the standard visual method (EN ISO 12945-4:2020), which is intuitive and cost-effective but better suited for evaluating more pronounced surface phenomena, such as pilling. This is mainly because fuzzing is usually accompanied by pilling, and their simultaneous occurrence makes separate analysis difficult. As a result, instrumental methods for assessing fuzzing that provide a more objective evaluation are rarely reported. In this research, an advanced digital imaging assessment method was introduced, using an innovative apparatus that, with simultaneous assessment of pilling, enabled separate digital imaging of the same textile fabric specimen’s surface fuzzing through a refined viewing angle. Additionally, newly developed software enabled digital analysis and acquisition of quantitative numerical values related to surface fuzzing. The research was conducted on six single-component woven fabrics made from cotton, wool, viscose, polyamide 6.6, polyester, and acrylic. Fuzzing was induced using an ICI tester (EN ISO 12945-1:2020) and a Martindale tester (EN ISO 12945-2:2020) through predefined box revolutions and fuzzing rubs ranging from 125 to 30,000. Fuzzing was assessed using both the standard visual method and the advanced digital imaging assessment method, with grading according to established classes based on the percentage change in fuzzing layer height. The results highlight the applicability of the advanced digital assessment method, as it separately captures the occurrence of fuzzing and distinguishes it from pilling. Full article
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25 pages, 18288 KB  
Article
Infill Pattern-Dependent Mechanical Properties and In Vitro Release Behavior of FDM 3D-Printed Resveratrol Amorphous Solid Dispersion Matrix Tablets
by Lianghao Huang, Kai Zheng, Xiaofeng Chen, Yunping Zhao, Tiantian Yang, Hang Yu, Wei Zhao, Xia Zhao and Jiaxiang Zhang
Polymers 2026, 18(12), 1531; https://doi.org/10.3390/polym18121531 - 19 Jun 2026
Viewed by 544
Abstract
Resveratrol (RSV) is a poorly water-soluble polyphenolic compound with various potential health benefits, but its pharmaceutical application is limited by low aqueous solubility and poor oral bioavailability. Additive manufacturing (AM), particularly fused deposition modeling (FDM) 3D printing, offers a flexible approach for fabricating [...] Read more.
Resveratrol (RSV) is a poorly water-soluble polyphenolic compound with various potential health benefits, but its pharmaceutical application is limited by low aqueous solubility and poor oral bioavailability. Additive manufacturing (AM), particularly fused deposition modeling (FDM) 3D printing, offers a flexible approach for fabricating oral dosage forms with customized geometry and internal architecture. In this study, hot-melt extrusion (HME) combined with fused deposition modeling (FDM) 3D printing was used to prepare RSV-loaded tablets with different infill patterns. Hydroxypropyl methylcellulose acetate succinate and hydroxypropyl cellulose were selected as polymeric carriers to prepare RSV-loaded filaments suitable for FDM printing. The effects of infill pattern on the solid-state characteristics, dimensional accuracy, mechanical properties, floating behavior, and in vitro drug release of the printed tablets were systematically investigated. Differential scanning calorimetry, powder X-ray diffraction, and polarized light microscopy indicated that RSV was mainly converted into an amorphous or molecularly dispersed state after HME and FDM processing. All designed tablets were successfully printed and showed acceptable shape fidelity, while different infill patterns resulted in variations in tablet weight, mechanical strength, floating duration, and release behavior. In vitro dissolution studies showed that the RSV release profiles were dependent on the internal infill architecture. Tablets with more complex infill patterns generally exhibited slower drug release, which may be related to differences in internal pore structure, medium penetration pathways, matrix hydration, and diffusion distance. Release kinetic analysis further suggested that RSV release from the printed tablets involved a combination of diffusion and polymer relaxation processes. These results demonstrate that infill pattern is an important structural parameter for modulating the mechanical performance and drug release behavior of FDM 3D-printed RSV tablets. This study provides useful guidance for the design of 3D-printed oral dosage forms with tunable release characteristics. Full article
(This article belongs to the Special Issue Advancements in Polymeric Materials for Precision Drug Delivery)
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22 pages, 32128 KB  
Article
Atomistic Mechanisms of Silicone Rubber Degradation Under Coupled Temperature–Humidity–Electric Field Conditions
by Yiheng Zhou, Zhijun An, Yixin He, Cong Qian, Qiuhua Zhou, Wentian Zeng, Xinhan Qiao and Wenyu Ye
Polymers 2026, 18(12), 1530; https://doi.org/10.3390/polym18121530 - 19 Jun 2026
Viewed by 700
Abstract
Silicone rubber is an important external insulating material for composite bushings, composite insulators, and other power equipment. During long-term service, it is inevitably exposed to coupled environmental and electrical stresses, such as elevated temperature, moisture ingress, strong electric fields, and partial discharge, which [...] Read more.
Silicone rubber is an important external insulating material for composite bushings, composite insulators, and other power equipment. During long-term service, it is inevitably exposed to coupled environmental and electrical stresses, such as elevated temperature, moisture ingress, strong electric fields, and partial discharge, which may lead to hydrophobicity loss, surface chalking, crack propagation, and particle shedding. To reveal the microscopic degradation mechanism of silicone rubber under complex operating conditions, a molecular model of methyl vinyl silicone rubber was constructed using Materials Studio. A stable silicone rubber molecular structure was obtained through crosslinking, geometry optimization, and ensemble relaxation. Subsequently, a reactive molecular dynamics simulation system under coupled temperature–humidity–electric field conditions was established using LAMMPS and the ReaxFF reactive force field. Different temperature gradients, electric field intensities, and aging–recovery stages were designed to investigate the degradation behavior of silicone rubber. The evolution of the maximum carbon content, maximum silicon content, carbon-containing decomposition products, and typical small-molecule products, including H2, H2O, CH4, C2H2, C2H4, and C2H6, was statistically analyzed. In addition, atomic trajectory tracking was performed to clarify the processes of methyl group detachment, Si-O bond cleavage, water molecule participation, and molecular chain reconstruction. The results show that high temperature mainly promotes methyl group detachment from side chains and fracture of the siloxane main chain, while a strong electric field accelerates the decomposition process and induces the transformation of long siloxane chains into shorter chains. Water molecules can react with broken siloxane chains to form hydroxyl-containing structures, making the structural degradation partially irreversible. The degradation process of silicone rubber under coupled temperature–humidity–electric field stress can be summarized as side-chain detachment, main-chain scission, water-assisted reactions, free-radical recombination, and local molecular aggregation. This study provides a molecular-level theoretical basis for aging mechanism analysis, condition assessment, and lifetime prediction of composite external insulating materials. Full article
(This article belongs to the Section Polymer Analysis and Characterization)
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18 pages, 17748 KB  
Article
Bio-Based Nanocellulose Cryogels Modified with Tannin and Vanillin: Intermolecular Interactions and Functional Properties
by Lincoln Audrew Cordeiro, Alessandro Zanchin, Elena Colusso, Camila Monteiro Cholant, Patricia Oliveira Schmitt, Radmila Rodrigues Gravato, Lorenzo Moro, Mara Vegro, Sarah Kalli Silva da Silva, Amanda Marcely Reis, Jonas Raphael Eckardt, Lorenzo Guerrini, André Luiz Missio and Gianluca Tondi
Polymers 2026, 18(12), 1529; https://doi.org/10.3390/polym18121529 - 19 Jun 2026
Viewed by 658
Abstract
Sustainable lightweight materials based on renewable resources have attracted increasing attention as alternatives to synthetic materials. However, developing nanocellulose cryogels with adequate structural integrity and efficient retention of phenolic compounds remains challenging, often requiring furanic and dialdehyde-based additives associated with environmental and health [...] Read more.
Sustainable lightweight materials based on renewable resources have attracted increasing attention as alternatives to synthetic materials. However, developing nanocellulose cryogels with adequate structural integrity and efficient retention of phenolic compounds remains challenging, often requiring furanic and dialdehyde-based additives associated with environmental and health concerns. In this context, tannin-containing nanocellulose cryogels were produced using vanillin and hydrogen peroxide as sustainable modification agents. The effects of the additives on the structural, morphological, colorimetric, mechanical, thermal, and leaching properties of the cryogels were investigated. FTIR and colorimetric analyses revealed the presence of phenolics and the effect of hydrogen peroxide. SEM analysis showed that tannin promoted structural densification, whereas peroxide induced fragmentation of the cryogel network and pore reorganization. These changes influenced density and mechanical performance, with nanocellulose-tannin exhibiting the highest compressive strength and elastic modulus. Thermal conductivity values remained within the range reported for highly porous lignocellulosic materials (38.93–43.79 (mW/m·K)). Tannin leaching demonstrated that peroxide significantly improved tannin retention, especially in the system including vanillin which exhibited only 13,61% tannin release. Overall, vanillin and hydrogen peroxide modified the supramolecular organization and functional properties of the cryogels, highlighting their potential as additives in porous materials for thermal insulation and adsorption applications. Full article
(This article belongs to the Section Biobased and Biodegradable Polymers)
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22 pages, 5273 KB  
Article
Structure–Property Relationships in PEI/PET Polymer Blends: Morphological, Rheological, Thermal, Mechanical Behavior, and Electromagnetic Response
by Elshod Olmosovich Khakberdiev, Hülya Kaftelen Odabaşı, Akın Odabaşı, Selcuk Helhel, Qodirbek Nuridin ugli Berdinazarov, Nizomiddin Zokir ugli Dusiyorov and Nigmat Rustamovich Ashurov
Polymers 2026, 18(12), 1528; https://doi.org/10.3390/polym18121528 - 19 Jun 2026
Viewed by 1101
Abstract
In this study, twin screw extruded Polyetherimide (PEI)/Poly(ethylene terephthalate) (PET) polymer blends (90/10, 70/30, 50/50 w/w%) were investigated to elucidate the composition–property relationship governed by morphological, structural, rheological, thermomechanical, mechanical, and electromagnetic shielding (EMI) performance behavior. Among other polymer blends, [...] Read more.
In this study, twin screw extruded Polyetherimide (PEI)/Poly(ethylene terephthalate) (PET) polymer blends (90/10, 70/30, 50/50 w/w%) were investigated to elucidate the composition–property relationship governed by morphological, structural, rheological, thermomechanical, mechanical, and electromagnetic shielding (EMI) performance behavior. Among other polymer blends, the 70/30 blend exhibits superior thermomechanical stability with a significant glass transition temperature of 132.7 °C, where a robust confinement effect effectively restricts the mobility of PET chains. This morphology, characterized by a domain size of 562 nm, provides proof of concept for interface-driven attenuation, reaching a maximum EMI shielding effectiveness of 2.54 dB within the investigated blends. This performance is primarily governed by Maxwell–Wagner–Sillars polarization at the immiscible boundaries, alongside an optimized dielectric loss of tan δ ≈ 0.065. The design of these high-temperature PEI blends provides a proof of concept for interface-driven attenuation and demonstrates their potential for developing advanced EMI shielding matrices. Full article
(This article belongs to the Section Polymer Chemistry)
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20 pages, 22758 KB  
Article
Ionic Liquid-Assisted Acetylated Xylan Coatings Reinforced with CuO and ZnO Nanoparticles for Food Packaging Papers
by Petronela Nechita and Silviu-Marian Năstac
Polymers 2026, 18(12), 1527; https://doi.org/10.3390/polym18121527 - 19 Jun 2026
Viewed by 482
Abstract
This study investigates the potential of xylan acetylated using imidazolium-based ionic liquids, particularly 1-ethyl-3-methylimidazolium acetate ([Emim]Ac), as a functional matrix for ZnO and CuO nanoparticles (ZnO NPs and CuO NPs) in composite coatings for food packaging paper. A single coating layer (approximately 5 [...] Read more.
This study investigates the potential of xylan acetylated using imidazolium-based ionic liquids, particularly 1-ethyl-3-methylimidazolium acetate ([Emim]Ac), as a functional matrix for ZnO and CuO nanoparticles (ZnO NPs and CuO NPs) in composite coatings for food packaging paper. A single coating layer (approximately 5 g/m2) was applied on both sides of the paper samples to improve barrier properties against water, oils, fats, and microbial contamination. The obtained results show that the combination of acetylated xylan with ZnO and CuO nanoparticles improved surface hydrophobicity, with contact angle values reaching 83° and 97°, respectively. The coatings exhibited antibacterial activity against Bacillus sp., as well as a reduction in fungal development of Penicillium spp., as evidenced by the observed inhibition of conidia sporulation. These findings indicate that ionic liquid-assisted acetylation of xylan using [Emim]Ac is an effective route for chemical modification of hemicelluloses. The developed xylan-based coatings demonstrate promising functional properties for potential application in sustainable food packaging materials, within the scope of the performed experiments. Full article
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Article
Sodium Caseinate/Tea Polyphenols Stabilized Lavender Essential Oil Nanoemulsions: Preparation, Characterization, Antibacterial Activity and Potential as Natural Food Preservatives
by Yu Chen, Jiaxin He, Haiting Cai, Yanli Cai, Wei Liao, Adem Gharsallaoui, Kai Yang, Peilong Sun, Ming Cai and Jian Wang
Polymers 2026, 18(12), 1526; https://doi.org/10.3390/polym18121526 - 19 Jun 2026
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Abstract
Excessive application of chemical preservatives has raised increasing concerns regarding food safety and human health, prompting the search for safer natural alternatives. Lavender essential oil (LEO), a plant-derived antimicrobial agent, has been considered a promising substitute for synthetic preservatives, but its high volatility [...] Read more.
Excessive application of chemical preservatives has raised increasing concerns regarding food safety and human health, prompting the search for safer natural alternatives. Lavender essential oil (LEO), a plant-derived antimicrobial agent, has been considered a promising substitute for synthetic preservatives, but its high volatility and poor water solubility limit its practical application. In this study, LEO nanoemulsions were fabricated via high-pressure homogenization using sodium caseinate (SC) and tea polyphenols (TPs) as composite emulsifiers. The preparation process was optimized using a three-factor, three-level orthogonal design, and the physicochemical properties, storage stability, and antibacterial activity were systematically investigated. The optimal preparation conditions were determined as an SC/TP mass ratio of 2:1, homogenization pressure of 70 MPa, and 7 homogenization cycles. The optimized nanoemulsion exhibited a droplet size of 130–210 nm, zeta potential of −30.89 mV, and encapsulation efficiency of 98.61%, with typical shear-thinning behavior and excellent storage stability. The percentage of free LEO remained below 7.5% within 15 days, indicating high stability, and the release behavior followed a zero-order kinetic model. The prepared nanoemulsion showed significant antibacterial activity against Staphylococcus aureus and Escherichia coli, with a minimum inhibitory concentration (MIC) of 62.5 μg/mL for both strains. This study confirms that the SC/TP composite interface can effectively stabilize LEO nanoemulsions, providing a theoretical basis for the development of natural and efficient food preservatives. Full article
(This article belongs to the Special Issue Biopolymers for Food Applications)
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