Search Results (430)

The utilization of polyethylene terephthalate (PET) waste from single-use packaging offers potential for sustainable manufacturing. This study evaluates recycled PET (rPET) from bottles as an FDM filament by varying infill architectures (honeycomb, gyroid, grid, and triangles) and layer thicknesses (0.20, 0.25, and 0.30 mm), with commercial PETG as a benchmark. Compared with previous rPET FDM studies, which were limited to reporting mechanical strength, the novelty of this study lies in the fact that it not only reports mechanical strength performance, but also compares printing time requirements and material efficiency. Efficiency calculations are obtained by comparing the weight of the filament to the weight of the printed specimen, which then correlates with optimizing processing time and costs. Overall, rPET produced densities of 1.11–1.22 g/cm³, tensile strengths of 12.5–22.5 MPa, flexural strengths of 12.5–30 MPa, impact strengths of 0.032–0.060 J/mm², and surface roughnesses of Ra 5.2–7.1 μm, while PETG showed higher mechanical performance (tensile 30–39.5 MPa, flexural 30–50 MPa, impact 0.037–0.065 J/mm²) and comparable density (1.15–1.27 g/cm³). Within rPET, gyroid provided the best optimal performance; the gyroid (0.20 mm) variation achieved the highest impact response (0.060 J/mm²) and the lowest Ra (5.2 μm) and the gyroid (0.25 mm) variation maximized flexural strength (30 MPa) and the gyroid (0.30 mm) variation maximized tensile strength (22.5 MPa). Material utilization efficiency was consistently higher for rPET (65–68%) than for PETG (46–56%). These results provide an integrated rPET-specific assessment and practical parameter recommendations for functional 3D printing, while also aligning with SDG 12 by pro-moting resource-efficient circular-economy practices through the utilization of waste materials in additive manufacturing. Full article

Sodium-ion batteries (SIBs) are considered a promising alternative to lithium-ion systems, with hard carbon (HC) being the most suitable anode material due to its disordered structure and increased interlayer distance. At the same time, the recycling of polyethylene terephthalate (PET), whose waste volumes are constantly growing, remains a pressing issue. In this work, recycled PET is used as a precursor for obtaining HC by direct carbonization at temperatures of 900–1400 °C. It is shown that the carbonization temperature significantly affects the structure and electrochemical properties of the obtained materials. The best characteristics were demonstrated by samples PET_1000 and PET_1100, which provided a high reversible capacity of 275–280 mAh g⁻¹ at a current density of 20 mA g⁻¹ in sodium-ion half-cells. The results confirm that controlled carbonization of recycled PET is an effective approach for obtaining highly efficient anode materials for SIBs and, at the same time, represents a promising way to utilize plastic waste. 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

Microplastic (MP) contamination in terrestrial ecosystems has emerged as a critical environmental concern, particularly in agricultural soils influenced by anthropogenic activities. This study investigated the depth-wise distribution, polymer composition, and associated ecological and human health risks of MPs in homestead agricultural soils across four regions of Bangladesh representing different levels of industrialization: Narayanganj (old industrial), Savar (moderate industrial), Gazipur (emerging industrial), and Mymensingh (non-industrial). Soil samples were collected from two depth intervals (0–20 cm and 21–50 cm), and MPs were extracted using density separation, identified through microscopic analysis, and characterized via ATR-FTIR spectroscopy. A diverse range of MP morphologies and polymers was detected, with irregular particles and fragments dominating the composition. Polypropylene (PP), high-density polyethylene (HDPE), and polyethylene terephthalate (PET) were the most abundant polymers, reflecting widespread domestic, industrial, and agricultural plastic usage. MP abundance was consistently higher in surface soils, indicating dominant surface inputs, although vertical migration into subsoil layers was evident. Spatial analysis revealed higher MP contamination in industrial regions, particularly Narayanganj and Savar, compared to the non-industrial reference site. Ecological risk assessment indicated low risk levels across all regions; however, significant spatial variability was observed. Human exposure assessment demonstrated that inhalation was the primary pathway, followed by dermal contact and ingestion, with children exhibiting higher exposure levels than adults. Lifetime average daily dose (LADD) and carcinogenic risk estimates remained below acceptable thresholds, suggesting minimal immediate health risks. Nevertheless, the persistence, mobility, and cumulative nature of MPs highlight potential long-term concerns. Therefore, this study provides comprehensive insights into the sources, distribution, and risks of MPs in homestead agricultural soils and underscores the need for improved waste management practices, sustainable agricultural strategies, and long-term monitoring to mitigate environmental and human health impacts. Full article

This review synthesizes current advances in the biocatalytic upcycling of plastic waste through microbial and enzymatic systems, emphasizing the transformation of recalcitrant polymers into high-value products. A narrative review methodology was adopted to integrate interdisciplinary findings across microbiology, enzymology, biotechnology, and waste management. Significant progress has been achieved in the depolymerization of plastics such as polyethylene terephthalate (PET), polyurethane, and polyolefins into intermediates, including terephthalic acid and ethylene glycol. These intermediates are subsequently valorized into products such as polyhydroxyalkanoates (PHAs), lipids, terpenoids, organic acids, aromatic compounds, and bacterial cellulose. Quantitative performance metrics demonstrate the potential of these systems. Notably, PHA production from PET-derived substrates has reached up to 1.10 g L⁻¹ (22.7% cell dry weight) and as high as 46% intracellular accumulation, while bacterial cellulose production from PET hydrolysates has achieved ~3.0 g L⁻¹. High conversion efficiencies have been reported in several pathways, including ~90–99% conversion of PET-derived intermediates to catechol, ~91.6% yield of glycolic acid from ethylene glycol (up to 31.4 g L⁻¹), and ~71–79% molar conversion of terephthalic acid to vanillin. Despite these advances, critical limitations persist, including low volumetric productivity in some systems, metabolic imbalances, substrate toxicity, feedstock heterogeneity, and challenges in process integration and scale-up. Future research should prioritize enhancing metabolic flux, improving enzyme efficiency, optimizing microbial consortia, and developing integrated, low-energy depolymerization–bioconversion systems. 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

The recycling of polyethylene terephthalate (PET) is gaining increasing importance, as it enables the conversion of plastic waste into valuable raw materials and contributes to a circular economy. Recent research has primarily focused on optimizing the depolymerization step of PET glycolysis, while downstream processes often overlook what are at least equally critical downstream steps in recovering the monomer bis(2-hydroxyethyl) terephthalate (BHET). The implementation of a water-free PET glycolysis process eliminates challenges related to internal solvent and homogeneous catalyst recycling that commonly occur in conventional processes. This study, therefore, focuses on BHET crystallization and filtration as key downstream unit operations. Two nucleation strategies, gassing and seeding, were investigated and compared with experiments without a nucleation strategy. The aim was to achieve reproducible process control during crystallization and to obtain crystals with good filterability, which can be critical for subsequent steps in the product purification process. Experiments without a nucleation strategy showed poor reproducibility. In contrast, gassing and seeding improved crystallization control, particularly regarding nucleation temperature and relative crystallization yield. However, these strategies also resulted in significantly prolonged filtration times due to differences in filter cake properties. The anisotropic crystals exhibited a broad particle size distribution with a high fraction of fine particles, leading to small and heterogeneous pores in the filter cake. Limited crystal growth was identified as the main cause of the unfavorable filtration behavior. Full article

In response to the growing demand for sustainable manufacturing, 3D printing using recycled polyethylene terephthalate (rPET) offers a novel waste-to-value conversion method. Although the application of rPET in additive manufacturing has attracted significant attention from both the academic and industrial sectors, substantial challenges impede its further development, notably the high processing shrinkage and poor mechanical properties of the final product. This study focuses on developing recycled PET-based composites with favorable processing, thermal, and mechanical properties. Regranulates were produced via twin-screw extrusion using PET flakes, multifunctional chain extenders, and short glass fibers (GFs). The rPET-GF composites were characterized in terms of their processing, thermal, thermomechanical, and mechanical properties. Epoxy-functional chain extender modification effectively increased the molecular weight and improved the processability, whereas GF reinforcement enhanced the tensile properties of both injection-molded and FDM-manufactured parts. A primary advantage of the rPET systems developed in this study is their delayed crystallization kinetics. These findings highlight the significant potential of the composites developed herein for extrusion-based additive manufacturing (MEX-AM), as delayed crystallization facilitates enhanced interfacial adhesion, lower volumetric shrinkage, and superior dimensional stability. Full article

Polyethylene terephthalate (PET) is among the most used plastics in domestic and industrial applications, particularly packaging, food containers and textiles. However, its recalcitrance to decomposition and biodegradation mostly results in landfilling and accumulation of PET waste in the environment if not processed. Chemical recycling of PET via selective depolymerization into its monomers may represent a pivotal step in the development of a truly circular economy of PET, which is still limited by economic and environmental sustainability issues. In this work, the depolymerization of PET is reported using ZnO as an insoluble catalyst, and ethanol as both a lytic agent and green solvent. A detailed investigation of reaction parameters, including reaction temperature, time and catalyst loading, showed that complete conversion of PET to diethyl terephthalate (DET) can be achieved with 92.5% selectivity at 180 °C and 48 h, with the potential for full DET selectivity at longer reaction times. The solid catalyst could be recovered and reused by simple centrifugation, with no loss of conversion or selectivity over three consecutive reuses. 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

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

Plastic pollution is a global environmental crisis, and microbial degradation represents a promising remediation strategy. While bacteria have been widely studied, yeasts offer unique advantages for plastic degradation due to their metabolic versatility, stress tolerance, and enzymatic capabilities. However, plastic degradative yeasts have not been reviewed comprehensively. Although several yeasts capable of degrading polyethylene terephthalate (PET) or polyethylene (PE) have been reported (e.g., Moesziomyces antarcticus, Candida tropicalis, Yarrowia lipolytica and Rhodotorula mucilaginosa), degraders of other plastic types are less studied. Although some yeasts can assimilate carbon from plastics, the diversity of yeasts capable of participating in plastic mineralization remains vastly underexplored. In recent years, yeast cell surface display systems for bacterial PETase and fungal cutinase have been developed, demonstrating promising PET degradation efficiency. However, PETase is feedback-inhibited by the intermediate product mono(2-hydroxyethyl)terephthalate (MHET). Systems synergizing PETase with MHETase have shown superior stability during long-term PET degradation and enable large-scale depolymerization of PET waste. For high-crystallinity PET, fungal hydrophobins can be used to modify the surface hydrophobicity of PETase-displaying yeast cells, facilitating their attachment to hydrophobic PET surfaces and ultimately enhancing the degradation efficiency of the whole-cell biocatalyst. Limitations of current research and future directions are also discussed. Full article

The management of plastic packaging waste needs to be optimized to improve recycling rates. In this article, fourteen categories of non-bottle polyethylene terephthalate (PET) packages were mechanically recycled at laboratory bench scale; the generated data were assessed using a multi-criteria decision analysis (MCDA) approach to identify the categories most suited for the mechanical recycling process from social, technical and legislative viewpoints. Recycling yields varied between 75% and 92% across the 14 categories. The intrinsic viscosity (IV) values of the produced recycled PET (rPET) corresponded to molecular weights ranging from 28,000 to 35,000 g/mol. The MCDA recyclability assessment showed that 7 of the 14 categories (accounting for 72% of the sorted products by mass flow) are often composed of multiple, inseparable materials, resulting in the lowest-quality rPET. Furthermore, only 4 categories (approximately 28% of the categories) were found suitable for closed-loop mechanical recycling. The stakeholders involved in the PET packaging value chain could use these results to support decision-making and the development of a well-organized framework to valorize even the most complex types of plastic waste. Full article

The incorporation of plastic waste into cement-based materials offers a promising strategy for improving sustainability; however, it is often associated with reduced mechanical performance due to weak interfacial bonding. This study investigates the effect of metakaolin on the interfacial transition zone (ITZ) and mechanical properties of cement mortars modified with polyethylene terephthalate (PET) flakes used for the partial replacement of natural sand. Mortars containing 10 and 50 wt% metakaolin (as cement replacement) and 5 vol.% PET flakes (as sand replacement) were prepared and tested after 28 days of curing. Compressive and flexural strength were evaluated, and microstructural analysis was conducted using scanning electron microscopy (SEM) with a focus on the ITZ. The results indicate that the incorporation of PET flakes leads to a reduction in mechanical properties due to the formation of a porous and weak ITZ. However, the addition of 10 wt% metakaolin significantly improved mechanical properties, enabling PET-modified mortars to achieve strength comparable to the reference mix. SEM observations revealed that metakaolin contributed to the refinement of the microstructure and reduction in ITZ porosity, which enhanced interfacial bonding and improved stress transfer between PET particles and the cement matrix. These findings demonstrate that metakaolin can effectively mitigate the negative effects associated with PET incorporation by improving the microstructural characteristics of the ITZ, thereby enhancing the performance of sustainable cement-based composites. Full article

The identification and characterization of air pollutants in metropolitan environments are of paramount global concern due to their significant implications for air quality and public health. This study investigates the chemical composition of fine particulate matter (PM_2.5) at two strategically selected urban sites in Seoul, South Korea, during 2020: Gwanghwamun Plaza, representing a high-density central location, and Bokjeong Station, situated in the metropolitan periphery. A key aspect of this research is the detection of terephthalic acid (TPA)—a distinct marker of polyethylene terephthalate (PET) combustion—using high-resolution liquid chromatography–time-of-flight tandem mass spectrometry (LC-ToF-MS/MS). Results from the simultaneous measurement campaign demonstrate that nighttime conditions strongly influence PM_2.5 at both sites, with increases observed not only in absolute concentrations (levoglucosan, TPA, As, CO, and NH₃) but also in OC-normalized ratios (levoglucosan/OC and TPA/OC). The consistent nighttime enhancement of these ratios suggests that the observed increases cannot be explained solely by reduced planetary boundary layer height but instead indicate relatively stronger emission contributions. These increases are likely influenced by waste incineration activities, wherein PET-based plastics and wood materials are combusted. Furthermore, assessment of the dithiothreitol assay-derived oxidative potential (DTT-OP) underscores the heightened oxidative stress associated with these emissions, posing substantial health risks. Full article