Search Results (370)

Plastic waste, particularly poly(ethylene terephthalate) (PET), negatively impacts the environment and human health. Biotechnology could become an alternative to managing PET waste if enzymes ensure the recovery of terephthalic acid with efficiencies comparable to those of chemical treatments. Recent research has highlighted the potential of fungal cutinases, such as wild-type ANCUT1 (ANCUT1^wt) from Aspergillus nidulans, in achieving PET depolymerization. Fungal cutinases’ structures differ from those of bacterial cutinases, while their PET depolymerization mechanism has not been well studied. Here, a reliable model of the ANCUT1^wt was obtained using AlphaFold 2.0. Computational chemistry revealed potential cation-binding sites, which had not been described regarding enzymatic activation in fungal cutinases. Moreover, it allowed the prediction of residues with the ability to interact with a PET trimer that were mutation candidates to engineer the substrate binding cleft, seeking enhancements of PET hydrolysis. Enzyme kinetics revealed that both ANCUT1^wt and ANCUT1^N73V/L171Q (DM) were activated by MgCl₂, increasing the dissociation constant of the substrate and maximal reaction rate. We found that in the presence of MgCl₂, DM hydrolyzed different PET samples and released 9.1-fold more products than ANCUT1^wt. Scanning Electron Microscopy revealed a different hydrolysis mode of these enzymes, influenced by the polymer’s crystallinity and structure. Full article

Polyethylene terephthalate (PET) is a widely used polymer whose accumulation in the environment poses a significant pollution challenge. This study explores the degradation of bis(2-hydroxyethyl) terephthalate (BHET) and terephthalic acid (TPA)—two monomers commonly produced during PET hydrolysis and widely used as intermediates in PET recycling—through Advanced Oxidation Processes (AOPs) employing KrCl (222 nm) and XeBr (283 nm) excimer lamps in the presence of hydrogen peroxide (H₂O₂). The effects of the H₂O₂/monomer mass ratio, initial monomer concentrations, and reaction volume on degradation efficiency were systematically evaluated. The results demonstrate that excimer lamp technology, particularly KrCl, holds promising potential for the effective degradation of both BHET and TPA, and thus represents a viable strategy for PET waste treatment. Full article

This study assessed the presence, abundance, and characteristics of microplastics (MPs) in farmed Pacific oysters (Crassostrea gigas) and evaluated the efficacy of depuration in reducing MPs under laboratory-controlled and commercial conditions. Oysters cultivated in the Lima estuary (NW Portugal) were sampled in autumn and winter, along with adjacent surface water and sediment, to investigate potential contamination sources. MP concentrations in oysters varied temporally, with higher levels in October 2023 (0.48 ± 0.34 MPs g⁻¹ ww) than in February 2024 (0.09 ± 0.07 MPs g⁻¹ ww), while the environmental levels remained stable across dates. All MPs were fibres, predominantly transparent, followed by blue and black. Fourier-Transform Infrared Spectroscopy (FTIR) confirmed cellulose and polyethylene terephthalate (PET) as dominant polymers in oysters and environmental samples. No clear correlation was found between MPs in oysters and surrounding compartments. Laboratory depuration reduced MPs by 78% within 48 h, highlighting its potential as a mitigation strategy. However, depuration was less effective under commercial conditions, possibly due to lower initial contamination levels. These findings suggest that oysters may act as a vector for human exposure to MPs via seafood consumption. While depuration shows promise in reducing contamination, further research is needed to optimise commercial protocols and enhance the safety of aquaculture products. Full article

The development of a silane coupling agent with an aminopropyl structure as a nucleating agent for poly(ethylene terephthalate) (PET) is reported in this study. The tri–block oligomers nucleating agent was formed by 1,3-bis(3-aminopropyl)-1,1,3,3-tetramethyldisiloxane/oxalic acid/low molecular weight PET (LPOBD). It was subsequently cross-linked with tetraethyl orthosilicate to form LPOBD-T. Composites of LPOBD/PET and LPOBD-T/PET were prepared by melt blending, and their thermal and crystallization behaviors were analyzed using XRD, DSC, TG, and POM. The results indicated that not only did the triblock polymer nucleating agent LPOBD exhibit a strong nucleation effect, but the crosslinked LPOBD-T also demonstrated superior crystallization performance. Specifically, the crystallinity of the 1 wt% LPOBD-T/PET composite increased by 3.3%, the crystallization temperature rose by 21.1 °C, and the t_1/2 was reduced by 53 s. Moreover, the crystalline morphology was more uniform. These findings indicate that the tri-block oligomers synthesized from a silane coupling agent serve as effective nucleating agents for PET. Full article

Microplastics (MPs) have emerged as pervasive environmental contaminants due to their widespread presence across various ecosystems, including their use in single-use plastic food ware and table salt dispensers. This issue coincides with the presence of heavy metals in water sources in Doha, Qatar. Fourier Transform Infrared (FTIR) analysis revealed that the plastic plate and spoon were composed of polyolefin, with the spoon exhibiting additional peaks that indicated oxidation or the presence of additives. Thermogravimetric Analysis (TGA) revealed that the spoon exhibited higher thermal stability, retaining approximately 10% of its mass at 700 °C, than the plate, which retained 2%, indicating the presence of complex additives or contamination. MPs in food-grade salt samples were verified through filtration and Fourier Transform Infrared (FTIR) Spectroscopy, identifying polymers such as polyethylene (PE), polypropylene (PP), and polyethylene terephthalate (PET). These MPs likely stem from exposure to packaging or environmental contaminants. FTIR spectra confirmed the integrity of the polymers after treatment. Inductively Coupled Plasma–Optical Emission Spectroscopy (ICP-OES) analysis revealed varying levels of heavy metals in bottled and tap water, with notable findings including detectable arsenic and lead in both, higher calcium and magnesium in bottled water, and the presence of copper present in tap water only, highlighting potential health and infrastructure-related concerns. These results highlight the possible risks associated with exposure to MPs and heavy metals from everyday products and water sources, underscoring the need for enhanced regulatory oversight and safer material choices to ensure protection. Full article

The recycling of post-consumer plastics for food-contact applications is subject to stringent regulatory requirements, particularly with regard to the removal of potentially harmful non-intentionally added substances (NIAS). While polyethylene terephthalate (PET) recycling processes are already approved by the European Food Safety Authority (EFSA), there is a lack of guidance for other polymers like polystyrene (PS). This study aims to provide a scientific basis for assessing the decontamination efficiency required for recycled post-consumer PS in food-contact applications. As one of the first studies to propose a framework for PS decontamination assessment based on EFSA food-consumption data and conservative diffusion modeling, it contributes to filling this regulatory gap. First, European food-consumption data were analyzed to identify critical scenarios of the age-group-dependent intake of PS-packaged food. Based on this, a conservative migration model was applied using a one-dimensional diffusion simulation to determine the maximum allowable initial concentrations of NIAS in PS. The calculated values were then compared with published reference contamination levels to calculate the required cleaning efficiency. The combination of food-consumption values and the migration process showed that trays for fruits and vegetables are the most critical food-contact application for post-consumer PS recycling. The most stringent assumptions resulted in necessary decontamination efficiencies ranging from 92% for the smallest molecule, toluene (92.14 g/mol), to 42% for the largest molecule, methyl stearate (298.50 g/mol). The results provide a methodological basis for regulatory assessments and offer practical guidance for designing safe recycling processes, thereby supporting the circular use of PS in food packaging and building the basis for future regulatory assessments of other polymers, in line with the European Union Plastics Strategy and circular economy objectives. Full article

Polymer residues can be reused in civil construction by partially replacing mineral aggregates in concrete, thereby reducing the extraction of natural resources. This study aimed to evaluate the use of powdered poly (ethylene terephthalate) (PET) and polyethylene (PE) residues, accumulated in shaving-mill filters during the extrusion of multilayer films used in food packaging, in the production of sealing masonry blocks. The PET/PE residues were characterized by Fourier Transform Infrared Spectroscopy (FTIR), thermogravimetric analysis (TGA) and scanning electron microscopy (SEM). Cylindrical specimens were produced in which part of the sand, by volume, was replaced with 10, 20, 30, 40 and 50% polymer residue. The cylindrical specimens were evaluated for specific mass, water absorption and axial and diametral compressive strengths. The 10% content provided the highest compressive strength. This formulation was selected for the manufacture of concrete blocks, which were evaluated and compared with the specifications of ABNT NBR 6136:2014. The concrete blocks showed potential for applications without structural function and were classified as Class C. The results, in line with previous investigations on the incorporation of plastic waste in concrete, underscore the promising application potential of this strategy. Full article

This study identifies different polymers using their fluorescent data under various light wavelengths that ranged from 245 nm to 345 nm in 10 nm intervals. The primary goal of the proposed method is to select optimal wavelengths that can lead to the accurate identification of six polymers: polyamide 6 (PA6), polymethyl methacrylate (PMMA), polypropylene (PP), polystyrene (PS), high-density polyethylene (HDPE), and polyethylene terephthalate (PET). By examining the specific fluorescence emission patterns of these polymers, the study provides insight into how each material responds uniquely to different excitation light sources. The potential approach could streamline polymer identification in recycling applications or even in quality control and environmental monitoring, including microplastics. This approach could lead to improved accuracy in polymer classification, contributing to more efficient material sorting and processing. Full article

The increasing accumulation of plastic waste—especially from packaging and post-consumer sources—calls for the development of sustainable recycling strategies. Due to the challenges associated with sorting mixed waste, directly processing waste streams offers a practical approach. Polyethylene terephthalate (PET) and high-density polyethylene (HDPE) are common consumer plastics, but they are difficult to recycle together due to immiscibility and degradation. In mixed waste, recycled HDPE (r-HDPE) often contaminates the recycled PET (r-PET) stream. Additive manufacturing (AM) offers a promising solution to upcycle these mixed polymers into functional products with minimal waste. This study investigates the processing and characterization of r-PET/r-HDPE blends for AM, focusing on the role of compatibilizers in enhancing their properties. Blends were melt-compounded using a twin-screw extruder to improve dispersion, followed by direct pellet-based 3D printing. A compatibilizer (0–7 php) was incorporated to improve miscibility. Rheological testing showed that the 5 php compatibilizer optimized viscosity and elasticity, ensuring smoother extrusion. Thermal analysis revealed a 30 °C increase in crystallization temperature and a shift in decomposition temperature from 370 °C to 400 °C, indicating improved thermal stability. Mechanical testing showed a tensile strength of 35 MPa and 17% elongation at break at optimal loading. Scanning electron microscopy (SEM) confirmed reduced phase separation and improved morphology. This work demonstrates that properly compatibilized r-PET/r-HDPE blends enable sustainable 3D printing without requiring polymer separation. The results highlight a viable path for the conversion of plastic waste into high-value, customizable components, contributing to landfill reduction and advancing circular economy practices in polymer manufacturing. Full article

Polyethylene terephthalate (PET) is one of the most frequently used synthetic polymers and it plays a major role in plastic pollution in aquatic environments. As PET undergoes environmental degradation, it sheds microplastics and chemical leachates, which have an effect on microbial communities, including benthic cyanobacteria. This review focuses on the molecular processes by which PET microplastics and their associated leachate affect the growth, physiological performance, and ecological performance of benthic cyanobacteria. We explore how PET-derived compounds serve as carbon and energy sources or signaling molecules, possibly affecting photosynthesis, nitrogen fixation, or stress response pathways through changes in gene expression. Moreover, the function of PET leachates as environmental modulators of microbial community structure, generators of reactive oxygen species (ROS), and disruptors of hormonal and quorum sensing networks are also outlined. Knowledge of these interactions is essential for the evaluation of the wider ecological risks resulting from plastic pollution and the likelihood of cyanobacterial blooms in PET-polluted environments. This review synthesizes evidence on how PET microplastics and leachates act as carbon sources and stressors, modulating gene expression to promote benthic cyanobacterial growth and toxin production, potentially exacerbating ecological risks in polluted aquatic systems. Full article

Microplastics (MPs) are emerging contaminants that can significantly impact soil nutrient dynamics, particularly phosphorus (P) cycling, which is critical for maintaining soil fertility and ecosystem productivity. However, limited information is available on how different microplastic types and concentrations specifically influence phosphorus dynamics and microbial enzyme activity in soils. Microplastic contamination may alter P cycling by directly supplying phosphorus or indirectly influencing microbial activity and enzyme function through changes in soil structure and aggregation. This study examined the short-term impacts of three widely used microplastic polymers—polyethylene (PE), polypropylene (PP), and polyethylene terephthalate (PET)—on soil phosphorus forms and alkaline phosphatase activity (APA), a key enzyme in phosphorus transformation. Incubation experiments were conducted at two concentrations (0.5% and 5%) over 30 and 60 days. The results indicated that the impact of microplastics on soil phosphorus dynamics varied according to both polymer type and contamination dose. Microplastics increased available phosphorus (AP) and APA levels compared to control soils, indicating a stimulatory effect on microbial processes. This may be due to the temporary accumulation of phosphorus on MP surfaces, which can stimulate phosphatase activity. Over time, however, both AP and APA levels declined, suggesting that degradation products released from MPs and organic matter may have altered the activity of the microbial communities responsible for P cycling. FTIR analysis revealed clear degradation of microplastics, with PET showing the most pronounced chemical transformation. PP exhibited moderate degradation, while PE demonstrated the highest resistance to environmental breakdown. These degradation processes likely released functional groups (e.g., carboxyl, carbonyl, hydroxyl) and low-molecular-weight compounds into the soil, modifying microbial processes and phosphorus chemistry. Particularly in PET-amended soils, these degradation products may have enhanced phosphate complexation or mobilization, contributing to higher levels of available phosphorus at the end of the incubation time. Understanding the polymer-specific and concentration-dependent effects of microplastics is critical for accurate ecological risk assessment in terrestrial ecosystems. Full article

This study investigates the fabrication of sustainable polymer-based floor tiles utilizing recycled high-density polyethylene, low-density polyethylene, polypropylene, and polyethylene terephthalate. The process incorporates rice husk ash and natural sand to create eco-friendly construction materials. The materials underwent assessment for density, water absorption, flexural strength, compressive strength, and abrasive wear. The results reveal a density range from 1.07051 to 1.6151 g/cm³, and water absorption ranging between 0.1996% and 0.68434%. Optimal flexural and compressive strengths were observed for HD70R15S1 and PET70R15S15, reaching 5.96 and 24.7933 MPa, respectively. Three-body abrasive wear testing indicates a minimum of 0.03095 cm³ for PET70R15S15 and a maximum of 0.17896 cm³ for HD70R15S15 composites. Full article

The rapid increase in plastic production and consumption has intensified research into human exposure to micro- and nanoplastics (MNPs) and their health effects. This study quantitatively assessed MNP internal exposure levels in non-invasive human samples, focusing on the four most common types of MNPs (≥300 nm): polyethylene terephthalate (PET), polypropylene (PP), low-density polyethylene (LDPE), and polystyrene (PS). Urine samples from 18 volunteers (4 males, 14 females) were analyzed using pyrolysis–gas chromatography–mass spectrometry (Py-GC/MS) with P(E-¹³C₂) as an internal standard. The study developed a straightforward yet effective analytical approach for quantifying MNPs in biological fluids. MNPs were detected in all urine samples, with concentrations ranging from 0.098 to 0.986 μg/mL and an average concentration of 0.268 ± 0.235 μg/mL. LDPE, 0.074 μg/mL (interquartile range: 0.030–0.243 μg/mL), was the most abundant polymer, accounting for 67.72% of the total MNPs, followed by PS at 21.17%, while PP and PET accounted for 7.06% and 4.05%, respectively. The results also suggest that drinking water type may serve as a distinct source of MNPs in urine. This study provides novel evidence on MNP (≥300 nm) internal exposure in humans and the influence of drinking habits, highlighting the application prospects of this method in assessing the potential health risks of MNPs. Full article

When testing the output of piezoelectric devices under different pressures, the friction between the pressure platform and the device causes a large amount of frictional electrical signals to be mixed in the output piezoelectric signal, seriously affecting the measurement accuracy of the piezoelectric signal. The current solution is to encapsulate the contact interface with identical materials to suppress triboelectric interference. However, this work has shown that even when contact separation is implemented at the interface of same media, triboelectric signals can still be generated. The heterogeneous potential distribution of the same material in contact separation has been discovered for the first time through the contact interface potential distribution, proving that charge transfer still exists between the same materials. Atomic force microscopy (AFM) was used to analyze the microstructure of the interface, and it was found that the existence of the surface tip structure would enhance the electron loss. Based on this, a new electron transfer model for surface–tip electron cloud interaction is proposed in this work. In addition, by comparing the output voltage characteristics of the triboelectric nanogenerators (TENGs) of seven polymer materials (e.g., polypropylene (PP), polyethylene (PE), polyvinyl chloride (PVC), polytetrafluoroethylene (PTFE), polyoxymethylene (POM), polyimide (PI), and polyethylene terephthalate (PET)), it was found that the open circuit voltage of PP material was only 0.06 V when they friction with each other, which is 2–3 orders of magnitude lower than other materials. When PP materials are applied to the package of piezoelectric devices, the precision of piezoelectric output characterization can be improved significantly, and a new experimental basis for a triboelectric theory system can be provided. Full article

Riverbed sediments act as potential retention reservoirs or transport corridors for microplastic particles (MPs) from river water to groundwater. Vertical concentration profiles of MPs, together with river water and groundwater analysis, provide insight into their fate and transport behavior in freshwater systems. However, such data remain scarce. This study provides a depth-specific analysis of MPs ≥ 100 µm (abundance, type, and size) in gravelly riverbed sediments down to 200 cm, along with river water and groundwater analysis. Three sediment freeze cores were collected from the Alpine Rhine, a channelized mountain stream with high flow velocities and permanent losing stream conditions. The average MP abundance in the riverbed was 3.1 ± 2.3 MP/kg (100–929 µm); in the river, 92 ± 5 MP/m³ (112–822 µm); and in the groundwater, 111 ± 6 MP/m³ (112–676 µm). The dominant polymer types in the riverbed were polypropylene (PP), polyvinyl chloride (PVC), and polyethylene terephthalate (PET) (>70%), while polyamide (PA) dominated in the river water (56%) and the groundwater (76%). The comparable MP concentration, particle sizes, and polymer types between river water and groundwater, as well as the vertical MP concentration profiles, indicate that even large MPs up to 676 µm are transported from river water to groundwater without significant retention in the gravel sediment. Full article