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Integrated Approach to Eco-Friendly Thermoplastic Composites Based on Chemically Recycled PET Co-Polymers Reinforced with Treated Banana Fibres

Authors :
UCL - SST/IMCN/BSMA - Bio and soft matter
University of Yaounde - Macromolecular Chemistry Unit
UCL - SST/IMMC/IMAP - Materials and process engineering
Kuete, Martial
Van Velthem, Pascal
Ballout, Wael
Nysten, Bernard
Devaux, Jacques
Ndikontar, Maurice Kor
Pardoen, Thomas
Bailly, Christian
UCL - SST/IMCN/BSMA - Bio and soft matter
University of Yaounde - Macromolecular Chemistry Unit
UCL - SST/IMMC/IMAP - Materials and process engineering
Kuete, Martial
Van Velthem, Pascal
Ballout, Wael
Nysten, Bernard
Devaux, Jacques
Ndikontar, Maurice Kor
Pardoen, Thomas
Bailly, Christian
Source :
Polymers, Vol. 14, no.22, p. 4791 (2022)
Publication Year :
2022

Abstract

A major societal issue of disposal and environmental pollution is raised by the enormous and fast-growing production of single-use polyethylene terephthalate (PET) bottles, especially in developing countries. To contribute to the problem solution, an original route to recycle PET in the form of value-added environmentally friendly thermoplastic composites with banana fibres (Musa acuminata) has been developed at the laboratory scale. Banana fibres are a so far undervalued by-product of banana crops with great potential as polymer reinforcement. The melt-processing constraints of commercial PET, including used bottles, being incompatible with the thermal stability limits use of natural fibres; PET has been modified with bio-sourced reactants to produce co-polymers with moderate processing temperatures below 200°C. First, commercial PET were partially glycolyzed with 1.3-propanediol to produce co-oligomers of about 20 repeating units, which were next chain extended with succinic anhydride and post-treated in a very unusual “soft solid state” process at temperatures in the vicinity of the melting point to generate co-polymers with excellent ductility. The molar mass build-up reaction is dominated by esterification of the chain ends and benefits from the addition of succinic anhydride to rebalance the acid-to-hydroxyl end-group ratio. Infra-red spectroscopy and intrinsic viscosity were extensively used to quantify the concentration of chain ends and the average molar mass of the co-polymers at all stages of the process. The best co-polymers are crystallisable, though at slow kinetics, with a Tg of 48°C and a melting point strongly dependent upon thermal history. The composites show high stiffness (4.8 GPa at 20% fibres), consistent with the excellent dispersion of the fibres and a very high interfacial cohesion. The strong adhesion can be tentatively explained by covalent bonding involving unreacted succinic anhydride in excess during solid stating. A first approach to

Details

Database :
OAIster
Journal :
Polymers, Vol. 14, no.22, p. 4791 (2022)
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1372941307
Document Type :
Electronic Resource