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Polyethelene terephthalate (PET) is a well-known thermoplastic, and recycling PET waste is important for the natural environment and human health. This study provides a comprehensive overview of the recycling and reuse of PET waste through energy recovery and physical, chemical, and biological recycling. This article summarizes the recycling methods and the high-value products derived from PET waste, specifically detailing the research progress on regenerated PET prepared by the mechanical recycling of fiber/yarn, fabric, and composite materials, and introduces the application of PET nanofibers recycled by physical dissolution and electrospinning in fields such as filtration, adsorption, electronics, and antibacterial materials. This article explains the energy recovery of PET through thermal decomposition and comprehensively discusses various chemical recycling methods, including the reaction mechanisms, catalysts, conversion efficiencies, and reaction products, with a brief introduction to PET biodegradation using hydrolytic enzymes provided. The analysis and comparison of various recycling methods indicated that the mechanical recycling method yielded PET products with a wide range of applications in composite materials. Electrospinning is a highly promising recycling strategy for fabricating recycled PET nanofibers. Compared to other methods, physical recycling has advantages such as low cost, low energy consumption, high value, simple processing, and environmental friendliness, making it the preferred choice for the recycling and high-value utilization of waste PET.
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http://dx.doi.org/10.1016/j.envres.2024.118428 | DOI Listing |
ACS Electrochem
September 2025
School of Chemistry, University of Nottingham, University Park, Nottingham NG7 2RD, UK.
The study of electrochemical oxidations has wide-ranging implications, from the development of new electrocatalysts for fuel cells for energy conversion, to the synthesis of fine chemicals. 2,2,6,6-Tetramethylpiperidine-1-oxyl (TEMPO) has been used for decades as a sustainable, metal-free mediator for chemical oxidations and is now being used for electrochemical oxidations. We describe here a novel approach to TEMPO-mediated electrooxidations, in which the chemical input and waste generated during electrooxidations of alcohols are minimized by using a multifunctional room temperature ionic liquid (RTIL) to facilitate flow electrosynthesis.
View Article and Find Full Text PDFBeilstein J Nanotechnol
September 2025
Faculty of Chemical Engineering, Industrial University of Ho Chi Minh City, Vietnam.
Effective removal of trace heavy metal ions from aqueous bodies is a pressing problem and requires significant improvement in the area of absorbent material in terms of removal efficiency and sustainability. We propose an efficient strategy to enhance the adsorption efficiency of carbon nanotubes (CNTs) by growing dendrimers on their surface. First, CNTs were pre-functionalized with maleic acid (MA) via Diels-Alder reaction in presence of a deep eutectic solvent under ultrasonication.
View Article and Find Full Text PDFRSC Adv
September 2025
Instituto de Ciencia de Materiales de Madrid, ICMM-CSIC C/Sor Juana Inés de la Cruz, 3 Madrid 28049 Spain
Perovskite light-emitting diodes (PeLEDs) have emerged as a promising technology for next-generation display and lighting applications, thanks to their remarkable colour purity, tunability, and ease of fabrication. In this work, we explore the incorporation of plasmonic spherical nanoparticles (NPs) directly embedded into the green-emitting CsPbBr perovskite layer in a PeLED as a strategy to enhance both its optical and electrical properties. We find that plasmonic effects directly boost spontaneous emission while also influencing charge carrier recombination dynamics.
View Article and Find Full Text PDFFront Microbiol
August 2025
Key Laboratory for Waste Plastics Biocatalytic Degradation and Recycling, College of Biotechnology and Pharmaceutical Engineering, Nanjing Tech University, Nanjing, China.
Polyurethane (PU), a segmented block copolymer with chemically resistant urethane linkages and tunable architecture, presents persistent biological recycling challenges. This study presents a Bacterial Laccase-Mediated System (BLMS) derived from for efficient degradation of polyester- and polyether-PU. Utilizing the laccase CotA and mediator 2,2'-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), the BLMS demonstrated effective de polymerization of both commercial and self-synthesized PU foams, including polyester- and polyether-types.
View Article and Find Full Text PDFChem Sci
August 2025
State Key Laboratory of Polymer Science and Technology, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences Changchun 130022 China
Poly(glycolic acid) (PGA) is one of the most widely used biodegradable polyesters, but its efficient valorization presents a long-standing challenge. Herein, we report the first facile PGA valorization strategy by utilizing epoxides to upcycle PGA into fused lactones under mild conditions (<100 °C), and subsequent copolymerization to produce copolyesters with wide potential tunability and enhanced performance. In the presence of epoxides and a chromium-based catalyst, PGA was efficiently transformed into fused lactones with a wide range of potential structural adjustability.
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