Search Results (353)

Bruxism-induced wear and microbial colonization of oral splints remain significant challenges in restorative dentistry. In this study, we developed a series of antibacterial nanocomposites based on a poly(ethylene terephthalate-co-1,4-cyclohexanedimethylene terephthalate) (PET-G) matrix incorporated with zinc oxide (ZnO) particles (3, 7, and 10 wt%), designed for the next generation of oral appliances. The composites were fabricated via a solvent-casting method followed by thermal processing. Differential scanning calorimetry (DSC) revealed that the amorphous nature and glass transition temperature (Tg ≈ 80 °C) of the PET-G matrix remained stable, ensuring excellent processability. While a minor decrease in Shore D hardness and flexural strength (up to 15%) was observed due to filler-induced structural discontinuity, the mechanical integrity remained within clinically acceptable limits. Crucially, the PET-G/ZnO composites exhibited potent antimicrobial activity; the 7 and 10 wt% loadings achieved a 100% reduction in Streptococcus oralis viability and significant inhibition of Candida albicans. These findings demonstrate that ZnO integration provides a dual-functional advantage—maintaining the thermoplastic versatility of PET-G while introducing critical bioactive properties, positioning these materials as a superior alternative for effective long-term bruxism therapy. Full article

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

Glycolysis of poly(ethylene terephthalate) (PET) offers a promising route for chemical recycling, yet conventional homogeneous catalysts often suffer from low selectivity, severe side reactions (especially diethylene glycol, DEG formation), and detrimental metal residues that compromise the quality of recycled products. To address these challenges, we herein develop dipotassium phenylphosphonate (PPOA-K) as an efficient homogeneous catalyst for PET glycolysis. Under optimized conditions (1 wt% catalyst, 197 °C, EG/PET mass ratio 3:1, 90 min, atmospheric pressure), PPOA-K achieves 100% PET depolymerization and a high BHET yield of 86.0%, and the reaction follows apparent first-order kinetics with an activation energy of 70.3 kJ·mol⁻¹. Beyond its high catalytic activity, PPOA-K effectively suppresses the acid-catalyzed etherification of ethylene glycol to DEG, a common side reaction that reduces monomer purity and degrades recycled polyester properties. Remarkably, the trace amount of PPOA-K remaining in the recovered BHET (17.3 ppm) is not detrimental; instead, it continues to inhibit DEG formation during repolymerization and acts as a thermal stabilizer, improving the melting point and thermal stability of recycled PET. The advantages of PPOA-K are further demonstrated in a partial (in situ) glycolysis–repolymerization process, where it reduces the DEG content in the final rPET to 1.78% (vs. 2.25% for conventional Zn(OAc)₂), yielding rPET with a higher melting point, higher crystallinity, and better color. This work demonstrates that dipotassium phenylphosphonate uniquely combines high catalytic activity, side reaction suppression, and beneficial residue effects, offering a new catalyst design strategy for high-quality PET recycling. Full article

A thermoreversible dynamic covalent network was constructed in recycled polyethylene terephthalate (RPET) via Diels–Alder (DA) chemistry to enhance mechanical performance, reprocessability, and self-healing. Furan-functionalized RPET (RPET-3F) was first prepared from maleated RPET (RPET-MA), followed by crosslinking with bismaleimide (BMI) at different feed ratios. FTIR spectra confirmed the successful grafting of furan groups and the formation of DA adducts. With increasing BMI content, the gel fraction and crosslink density increased substantially, whereas the swelling ratio decreased, indicating the progressive development of a three-dimensional network. RPET-3F-2B showed the highest network integrity among all samples. DSC analysis revealed a distinct retro-DA dissociation peak at 143 °C and a recrosslinking peak near 124 °C, confirming the thermal reversibility of the DA network. Owing to the optimized network structure, RPET-3F-2B exhibited the best mechanical properties and excellent reprocessability, retaining stable performance after three hot-pressing cycles. After repeated reprocessing, its tensile strength remained 74% higher than that of RPET-MA, while the elongation at break was still improved by about 10%. Moreover, the sample showed efficient thermally induced self-healing at 150 °C, with surface cracks nearly disappearing after 4 h. These results demonstrate that DA chemistry offers a promising route to the high-value reutilization of RPET into recyclable, multifunctional polymer materials. Full article

Microplastics (MPs) are pervasive contaminants that have been detected throughout the food chain. Their presence raises concerns in foods intended for health-related purposes, as these products are often consumed by vulnerable populations such as infants, older adults, and patients requiring clinical nutrition support. These groups may be more susceptible to contaminant exposure and may rely heavily on specialized foods. Therefore, understanding the occurrence and potential risks of MPs in such products is important. This review summarizes the current state of knowledge regarding the presence, sources, and health implications of plastic particles in several categories of health-oriented foods, including dietary supplements, medicinal herbs, plant-based beverages, honey, infant formulas, and clinical nutrition products, including enteral and parenteral formulations. Microplastics have been reported across these matrices. Fibers and fragments dominate, and common polymers include polyamide, polyethylene, polypropylene, and poly(ethylene terephthalate). These particles can originate from polluted water, soil, and air, as well as from production processes, packaging wear, and clinical delivery systems. Current evidence suggests that improving methodological consistency and expanding targeted toxicological research relevant to vulnerable populations will be crucial for strengthening risk assessment. Full article

Aerogels were produced exclusively from recycled plastic bottles of poly(ethylene terephthalate) (rPET) by optimising a dissolution–precipitation process at room temperature and applying a product design strategy to improve their sustainability. Using a design of experiments methodology, the systematic assessment of the influence of different factors, namely rPET concentration, co-solvent ratio, and non-solvent quantity, on the key properties of rPET aerogel, namely bulk density, thermal conductivity, and mechanical resistance, was performed. The understanding of the significance of each parameter and the optimisation of a desirability function offered reliable optimum results for the adjustment of the experimental procedure for the reduction in the volume of the most critical solvent, trifluoroacetic acid (TFA), by 42.5%. The observed bulk density values were excellent, down to 110 kg·m⁻³, and the thermal conductivity was in the range of conventional commercial insulators (38 mW·m⁻¹·K⁻¹), positioning this material as a real alternative to conventional thermal insulators. Also, to deeply understand the dissolution/precipitation phenomena, molecular dynamics simulations were conducted to support the experimental outcomes. Full article

The exponential growth of the global textile industry, largely driven by the demand for synthetic polymers such as poly(ethylene terephthalate) (PET), polyamides, and polyurethanes, has led to severe environmental consequences, notably the accumulation of persistent microplastics and solid waste. While conventional mechanical and chemical recycling methods are widely employed, they are often hindered by harsh processing conditions and the deterioration of material properties. Consequently, there is a critical need for sustainable end-of-life management strategies. This review provides a comprehensive analysis of the biodegradability of synthetic textile fibres, with a primary focus on emerging biotechnological and enzymatic recycling approaches. It systematically examines the intrinsic polymer characteristics that govern biodegradation—including molecular orientation, crystallinity, functional groups, and fibre chemistry—as well as extrinsic factors such as textile finishings, yarn twist, polymer blends, and chemical additives. Furthermore, the current landscape of microbial and enzymatic degradation routes is critically assessed, highlighting the specific mechanisms of biocatalysts (e.g., lipases, cutinases, PETase, and MHETase) in depolymerising complex synthetic matrices into recoverable monomers. Finally, this review identifies the existing literature gap between bulk plastic and textile-specific biodegradation, discussing future perspectives. By bridging polymer science and textile engineering, this work underscores the potential of enzymatic recycling to close the loop in synthetic fibre production and advance the transition toward a circular economy. Full article

Achieving a circular and climate-neutral bioeconomy by 2050 requires not only high-quality recycling but also the large-scale integration of renewable carbon from biomass and atmospheric CO₂ into material systems. Plastics represent the world’s largest and most rapidly growing carbon sink, positioning them as a critical intervention point for replacing fossil-based feedstocks with renewable alternatives. Because plastic packaging is one of the most visible material streams encountered by consumers in daily life, a transition toward sustainable, recyclable bioplastics has the potential to deliver both meaningful environmental benefits and strong societal impact, accelerating public awareness and acceptance of renewable carbon solutions. Poly(ethylene furanoate) (PEF)—a fully bio-based polyester synthesized from plant-derived 2,5-furandicarboxylic acid (FDCA) and monoethylene glycol (MEG)—offers a promising pathway toward more sustainable packaging due to its superior mechanical strength and gas-barrier performance relative to polyethylene terephthalate (PET). This study presents a cradle to grave life cycle assessment (LCA) of PEF resin production and PEF bottle applications, using industrially relevant, at-scale process data covering biomass feedstock conversion, polymer synthesis, packaging manufacture, use phase, and end of life. Bottle applications were selected as a focal point due to their technical maturity, commercial relevance, and suitability for direct comparison with incumbent PET systems. The results indicate that PEF can reduce greenhouse gas emissions by up to 71% and fossil resource depletion by 26% compared to PET at the resin level when biogenic carbon uptake is included. Moreover, the material’s enhanced functional properties enable lightweight, recyclable bottle designs with carbon footprint reductions of up to 88% for 500 mL formats under a baseline recycling rate scenario of 72%, with the remaining share directed to municipal solid-waste incineration with energy recovery. Sensitivity analyses reveal that virgin PEF maintains environmental advantages over PET even when PET incorporates high levels of recycled content, highlighting the complementary roles of renewable carbon and circular material strategies. Prospective scenario modeling underscores the importance of sustainable feedstock selection and process electrification, with sucrose-based routes offering the largest potential for further decarbonization. Overall, the findings demonstrate that PEF is a scalable biopolymer capable of delivering substantial climate benefits while supporting circularity objectives. By targeting a highly visible consumer application—plastic packaging—this transition amplifies the societal impact of adopting renewable carbon materials. The study provides actionable insights for policymakers, industry stakeholders, and sustainability practitioners working to advance a more resilient, renewable, and consumer-recognizable plastics economy. Full article

This study provides the first comprehensive assessment of microplastic (MP) contamination within oyster bed ecosystems of the Kingdom of Bahrain. Sediment, water, and oyster samples were collected from six sites representing diverse environmental conditions. Raman spectroscopy identified the presence of 12 distinct polymer types, with polypropylene (PP), polyurethane (PU), poly(ethylene terephthalate)/diamine/multi-walled carbon nanotube (PET/diamine/MWCNT), and fluorinated ethylene propylene (FEP) being the most prevalent. MPs occurred predominantly as fragments, films, and pellets, with black being the most common color across all matrices. MP abundances ranged from 750 to 1850 MPs/kg dry weight in sediments, 2100–9600 MPs/L in water, and 1.78–5.25 MPs/individual in oysters, with particles (<50 µm) most frequent in oyster tissues. Although spatial variation was evident across regions, detected polymers included types associated with known ecotoxicological risks. No significant correlation was observed between sediment grain size and MP abundance, suggesting that additional hydrodynamic or anthropogenic factors may influence MP distribution. Overall, this study provides critical baseline data on MP contamination in Bahrain’s marine environments and highlights the need for continued monitoring to assess potential risks to marine ecosystems and seafood safety. It also contributes to the limited understanding of MPs in the Arabian Gulf, informing future monitoring, conservation and policy initiatives that support long-term environmental sustainability. Full article

Plastic pollution caused by poly(ethylene terephthalate) (PET) highlights the urgent need for efficient biodegradation strategies. However, PET hydrolases such as DuraPETase typically exhibit limited substrate affinity for PET and insufficient operational stability. Although conventional immobilization improves enzyme stability, it often compromises catalytic activity. Here, we design a PET-targeting, orientation-controlled immobilization strategy that overcomes this traditional trade-off and enables efficient PET biodegradation. Guided by rational structural analysis, three Cys variants (R53C, R59C, R224C) were engineered for site-specific covalent attachment to a PDA@SiO₂ support with inherent PET-binding capability. The resulting conjugates (Dura_R53C-PDA@SiO₂, Dura_R59C-PDA@SiO₂, and Dura_R224C-PDA@SiO₂) displayed distinct catalytic and stability profiles. Among them, Dura_R59C-PDA@SiO₂ achieved the optimal balance between activity and stability, retaining kinetic properties comparable to the free enzyme and maintaining 87.6% residual activity after 2 h at 80 °C. Water contact angle measurements confirmed its PET-targeting behavior, as evidenced by the reduction in the PET contact angle from 85° to 45°. In 10-day degradation assays at 50 °C, Dura_R59C-PDA@SiO₂ released a total of 4865.32 μM degradation products, representing a 2.37-fold increase relative to free DuraPETase. These findings demonstrate an effective strategy for industrial enzymatic PET degradation and recycling. Full article

The increasing accumulation of poly(ethylene terephthalate) (PET) waste poses a significant environmental challenge and highlights the need for sustainable, value-added recycling strategies. In this study, porous carbon derived from PET was synthesized via carbonization and chemical activation and subsequently combined with manganese dioxide (MnO₂) to fabricate hybrid electrodes for aqueous supercapacitors. The PET-derived carbon exhibits a highly microporous structure with a large specific surface area and functions as a conductive and mechanically stable matrix that improves MnO₂ dispersion, charge transport, and electrochemical utilization. Systematic electrochemical investigations reveal strongly electrolyte-dependent charge-storage behavior. In an alkaline electrolyte, the capacitance is dominated by MnO₂ pseudocapacitive redox reactions, whereas in a neutral electrolyte, the response is primarily governed by electric double-layer charge storage. In a ferricyanide-containing redox-active electrolyte, additional electrolyte-mediated faradaic processes significantly enhance the apparent electrochemical performance. Under these conditions, the hybrid electrodes deliver a high apparent specific capacitance of 240–250 F g⁻¹ at moderate current densities. The electrodes further demonstrate stable cycling behavior and high apparent Coulombic efficiency, reflecting time-dependent utilization of both MnO₂ pseudocapacitance and redox-active electrolyte species during charge–discharge. Crucially, this work demonstrates that PET-derived carbon/MnO₂ hybrid electrodes exhibit complex, electrolyte-controlled charge-storage mechanisms and underscores the critical role of electrolyte selection in accurately interpreting electrochemical metrics and optimizing the performance of sustainable supercapacitors based on recycled polymer-derived carbons. Full article

Poly(ethylene terephthalate) (PET) composites reinforced with reduced graphene oxide (rGO) were investigated in order to elucidate the influence of nanofiller concentration and compatibilization on the viscoelastic relaxation behavior across the glass transition. Composites containing 0.1 and 0.5 wt% rGO were prepared by melt blending, and selected systems incorporated 5 wt% of an ionomeric polyester (PETi) as compatibilizer to enhance interfacial adhesion. The thermomechanical response was characterized using dynamic mechanical analysis (DMA) as a function of temperature. Experimental results revealed a strong dependence of stiffness, damping, and glass transition behavior on filler concentration and interfacial interactions. While low rGO loading produced minor changes, the incorporation of 0.5 wt% rGO significantly increased the glassy modulus and shifted the glass transition temperature, indicating restricted segmental mobility. Compatibilized systems exhibited further stiffness enhancement and modified relaxation dynamics due to improved stress transfer and interphase development. To capture the distributed nature of the relaxation processes, the glass transition region was modeled using a fractional Zener model (FZM) with two spring-pot elements within a cooperative relaxation framework. The model successfully reproduced the experimental $E^{\prime }$ and $tan\delta$ curves and revealed systematic variations in the fractional exponents and cooperative parameters. The results demonstrate that the introduction of rGO and compatibilizer progressively transforms the relaxation spectrum of PET from a relatively uniform segmental process into a heterogeneous, interfacially mediated viscoelastic response that is naturally described by fractional rheology. Full article

Materials derived from renewable and recycled resources offer a promising route toward more sustainable thermoset composites. In this study, waste poly(ethylene terephthalate) (PET) was depolymerized by glycolysis with propylene glycol to obtain a glycolysate, and subsequently polycondensed with biobased propylene glycol, maleic anhydride, and trimethylolpropane diallyl ether to synthesize biobased UV-curable unsaturated polyester resin (UV-bUPR). The composites were prepared with acryloyl-modified Kraft lignin (K_rL-A) as a reactive bio-filler using a dual-curing approach, in which rapid UV curing was followed by thermal/redox post-curing to improve conversion and network homogeneity. The structure of the synthesized resin and composites was confirmed by FTIR and NMR spectroscopy. Mechanical properties were evaluated by tensile testing and hardness measurements, while morphology and fracture behavior were analyzed by scanning electron microscopy. The unmodified lignin decreased tensile performance due to limited compatibility with the polyester matrix and the formation of interfacial defects and agglomerates. In contrast, K_rL-A exhibited improved dispersion and stronger filler–matrix interactions, resulting in superior mechanical performance. The most pronounced effect of lignin modification was observed at 15 wt.% filler loading, where the tensile strength reached 27.83 MPa, compared with 13.91 MPa for the corresponding unmodified system. The developed composites also showed improved sustainability, assessed through the E-factor, due to the combined use of recycled PET and renewable lignin. Full article

The development of selective and sustainable catalysts is essential to enable the chemical recycling of mixed plastic waste. In this work, calcium-modified biochars derived from cocoa pod husk (CPH) and palm kernel shell (PKS) were prepared for treating a mixture of poly(ethylene terephthalate) (PET) and poly(lactic acid) (PLA). The aim was to separate the mixture through the PLA methanolysis, while maintaining the PET unreacted for a potential physical recycling. Biochar was ex situ modified with calcium precursor using a value-added concentrate recovered from the hydrothermal treatment of Jatropha fruit husk. Subsequently, a pyrolysis step was further applied to convert the calcium species into CaO, which is the active phase for the methanolysis reaction. Structural, microscopic, and spectroscopic analyses revealed that the carbon matrix strongly influences the evolution and stabilization of calcium phases during pyrolysis and post-treatment. CPH-derived biochars promoted the formation of highly dispersed CaO, whereas PKS favored the growth of larger, less reactive Ca(OH)₂ domains. As a result, the CPH_Ca10 (i.e., 10% desired calcium loading based on CPH-biochar mass) catalyst exhibited superior basicity and catalytic activity, achieving near-complete PLA conversion under mild conditions (90–110 °C) depending on the system with only 2 wt.% catalyst. Importantly, under these mild conditions, PET remained chemically intact, demonstrating the process’s high selectivity and applicability to mixed bioplastic–fossil plastic streams. This study highlights a circular, low-carbon route to producing effective Ca-based catalysts from agricultural residues. It establishes a promising strategy for selective depolymerization and separation in complex plastic waste systems. Full article

Background: The ability of synthetic plastics to persist in the environment and the accumulation of microplastics has intensified the need to explore biological mechanisms capable of interacting with, and possibly degrading, polymeric materials. Microbial enzymes that have extensive catalytic flexibility represent promising candidates in this context. Aim: This study set out to examine the molecular interaction patterns and dynamical stability of Pseudomonas aeruginosa elastase (LasB) with representative structural fragments of typical synthetic plastics to assess the suitability of the enzyme to polymer-derived substrates. Methods: The crystallographic structure of LasB (PDB ID: 1EZM) was retrieved from the Protein Data Bank and pre-prepared with the help of AutoDock4.2.6 Tools. Those polymer-derived ligands that were associated with the major industrial plastics such as polyamide (PA), polyvinyl chloride (PVC), polycarbonate (PC), poly-ethylene terephthalate (PET), polymethyl methacrylate (PMMA), and polyurethane (PUR) were retrieved in the PubChem database and geometrically optimized with the help of the MMFF94 force field. AutoDock Vina, with a specific grid box around the catalytic pocket, including Zn²⁺ ion, was used to perform molecular docking simulations. PyMOL and BIOVIA Discovery Studio software were used to analyze binding conformations, interaction residues and types of intermolecular contacts. Phosphoramidon, a known metalloprotease inhibitor, served as a positive control to confirm the docking protocol. Additional assessment of the structural stability and conformational behavior of the enzyme–ligand complexes was conducted by molecular dynamics (MD) simulations with the Desmond engine and explicit solvent model in a 50 ns trajectory using the OPLS4 force field. RMSD, RMSF, radius of gyration, hydrogen bonding analysis and solvent accessibility parameters were used to measure structural stability. Results: The docking experiment showed varying binding affinities with the test polymers. Polycarbonate (−5.774 kcal/mol) and polyurethane (−5.707 kcal/mol) had the highest in-teractions with the LasB catalytic pocket, polyamide (−5.277 kcal/mol) and PET (−4.483 kcal/mol) followed PMMA and PVC, which had weaker affinities. The following were the important residues involved in interaction networks: Glu141, His140, Val137, Arg198, Tyr114, and Trp115 that were implicated in interaction networks with hydrophobic interactions, π-cation interactions and van der Waals forces that were the major stabilization forces. MD simulations had stabilized complexes, and RMSD values were found to be within acceptable ranges of stability, and ligand-specific changes (around 1.0-3.2 A), which is also in line with stable protein-ligand systems. Phosphoramidon used as a positive control had an RMSD of 1.205 A which is within this stability range. PCA determined various ligand-bound conformational states of LasB with PA in com-pact state, PC and PVC in intermediate states and PUR, PMMA and PET in ex-panded conformations, indicating structur-al stability and adaptability of the binding pocket. Conclusion: These findings show that LasB has a structurally flexible catalytic pocket that can accommodate a wide range of polymer-derived ligands. These results offer an insight into the recognition of enzymes with polymers at the molecular level and also indicate that LasB might help in the interaction of microorganisms with synthetic plastics in environmental systems. Full article