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Electrocatalytic valorization of PET plastic waste provides an appealing route by converting intermittent renewable energy into valuable chemicals and high-energy fuels. Normally, anodic PET hydrolysate oxidation and cathodic water reduction reactions occur simultaneously in the same time and space, which increases the challenges for product separation and operational conditions. Although these problems can be addressed by utilizing membranes or diaphragms, the parasitic cell resistance and high overall cost severely restrict their future application. Herein, we introduce a Ni(ii)/Ni(iii) redox mediator to decouple these reactions into two independent processes: an electrochemical process for water reduction to produce hydrogen fuel assisted by the oxidation of the Ni(OH) electrode into the NiOOH counterpart, followed subsequently by a spontaneous chemical process for the valorization of PET hydrolysate to produce formic acid with a high faradaic efficiency of ∼96% by the oxidized NiOOH electrode. This decoupling strategy enables the electrochemical valorization of PET plastic waste in a membrane-free system to produce high-value formic acid and high-purity hydrogen production. This study provides an appealing route to facilitate the transformation process of PET plastic waste into high-value products with high efficiency, low cost and high purity.
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http://dx.doi.org/10.1039/d4sc01613k | DOI Listing |
Food Chem
August 2025
Food Engineering and Technology Department, Institute of Chemical Technology, Matunga, Mumbai, India.
Coextraction of Citrullus lanatus seeds and Citrus aurantium peels (1:1, w/w), two food processing wastes, was performed using supercritical carbon dioxide (scCO) (345 bar|57 °C|178 min) and pet ether solvents. The major objective of the study was to valorize two fruit processing wastes to obtain a bioactive coextract using a green scCO extraction process and further incorporate it into wax-based composite oleofoams. The scCO coextraction resulted in better extraction of bioactive compounds such as d-limonene and polyunsaturated fatty acids due to the absence of light and lower temperature of extraction, compared to pet ether.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Key Laboratory of Photochemical Conversion and Optoelectronic Materials & CAS-HKU Joint Laboratory on New Materials, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190, P.R. China.
Photocatalytic upcycling of polyethylene terephthalate (PET) waste into value-added chemicals represents a sustainable route for plastic valorization. However, previous studies have solely focused on generating oxygenated compounds through intramolecular C─O bond transformations. Achieving heteroatom-containing important chemicals via intermolecular coupling reactions is still challenging.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2025
Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences (CAS), Guangzhou 510640, PR China; CAS Key Laboratory of Renewable Energy, Guangzhou 510640, PR China; Guangdong Provincial Key Laboratory of New and Renewable Energy Research and Development, Guangzhou 510640, PR China. Electroni
The widespread and uncontrolled disposal of polyethylene terephthalate (PET) plastics poses a significant environmental challenge. In this study, we propose a sustainable upcycling strategy to convert waste PET into high-value bimetallic nickel/cobalt-1,4-benzenedicarboxylate metal-organic frameworks (NiCo-BDC MOFs) via a one-pot solvothermal method. By tuning the Ni/Co precursor ratio, the morphology of the resulting NiCo-BDC transitions controllably from stacked nanowires to nanorods, forming a hybrid crystalline-amorphous architecture with a large specific surface area and well-developed hierarchical porosity.
View Article and Find Full Text PDFBiotechnol Adv
August 2025
Chemical Engineering Research Centre, School of Chemical Engineering and Technology, Tianjin University, Tianjin 300072, PR China; State Key Laboratory of Chemical Engineering and Low-Carbon Technology, Tianjin University, Tianjin 300072, PR China.
With excellent mechanical properties and chemical stability, poly (ethylene terephthalate) (PET), an engineering plastic, is widely applied in textiles and packaging. However, the widespread use and low biodegradability of PET have resulted in significant environmental pollution. Recent advances in PET hydrolase discovery and engineering have driven the rapid advancement of PET bio-recycling, while efficient PET hydrolases can depolymerize PET into monomers under mild conditions, providing a sustainable approach to potentially addressing the plastic pollution issue.
View Article and Find Full Text PDFMacromol Rapid Commun
July 2025
School of Chemical Sciences and Advanced Materials Research Center, Indian Institute of Technology Mandi, Mandi, Himachal Pradesh, India.
Human reliance on plastic has increased plastic waste generation. Polyethylene terephthalate (PET) is one of the major commodity plastics used and shows long persistence in nature, causing environmental threats. To mitigate this problem of pollution, a highly efficient ZnFe-layered double hydroxide has been synthesized via the hydrothermal method for valorization of waste PET bottles to bis(2-hydroxyethyl) terephthalate (BHET) by glycolysis.
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