Perspective on the Development of Monomer Recovery Technologies from Plastics Designed to Last.
Journal
ACS organic & inorganic Au
ISSN: 2694-247X
Titre abrégé: ACS Org Inorg Au
Pays: United States
ID NLM: 9918282981206676
Informations de publication
Date de publication:
07 Aug 2024
07 Aug 2024
Historique:
received:
31
01
2024
revised:
18
03
2024
accepted:
19
03
2024
medline:
12
8
2024
pubmed:
12
8
2024
entrez:
12
8
2024
Statut:
epublish
Résumé
In order to prevent the current unsustainable waste handling of the enormous volumes of end-of-use organic polymer material sent to landfilling or incineration, extensive research efforts have been devoted toward the development of appropriate solutions for the recycling of commercial thermoset polymers. The inability of such cross-linked polymers to be remelted once cured implies that mechanical recycling processes used for thermoplastic materials do not translate to the recycling of thermoset polymers. Moreover, the structural diversity within the materials from the use of different monomers as well as the use of such polymers for the fabrication of fiber-reinforced polymer composites make recycling of these materials highly challenging. In this Perspective, depolymerization strategies for thermoset polymers are discussed with an emphasis on recent advancements within our group on recovering polymer building blocks from polyurethane (PU) and epoxy-based materials. While these two represent the largest thermoset polymer groups with respect to the production volumes, the recycling landscapes for these classes of materials are vastly different. For PU, increased collaboration between academia and industry has resulted in major advancements within solvolysis, acidolysis, aminolysis, and split-phase glycolysis for polyol recovery, where several processes are being evaluated for further scaling studies. For epoxy-based materials, the molecular skeleton has no obvious target for chemical scission. Nevertheless, we have recently demonstrated the possibility of the disassembly of the epoxy polymer in fiber-reinforced composites for bisphenol A (BPA) recovery through catalytic C-O bond cleavage. Furthermore, a base promoted cleavage developed by us and others shows tremendous potential for the recovery of BPA from epoxy polymers. Further efforts are still required for evaluating the suitability of such monomer recovery strategies for epoxy materials at an industrial scale. Nonetheless, recent advancements as illustrated with the presented chemistry suggest that the future of thermoset polymer recycling could include processes that emphasize monomer recovery in an energy efficient manner for closed-loop recycling.
Identifiants
pubmed: 39132016
doi: 10.1021/acsorginorgau.4c00009
pmc: PMC11311459
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
373-386Informations de copyright
© 2024 The Authors. Published by American Chemical Society.
Déclaration de conflit d'intérêts
The authors declare the following competing financial interest(s): S.K.K., B.S.D., and T.S. are inventors of patent PCT/EP2023/058993 on the tert-amyl alcohol solvolysis process for deconstruction of polyurethane, submitted by Aarhus University. A.A. and T.S. are inventors on patent PCT/EP2022/156129 on the catalytic disconnection of C-O bonds in epoxy resins and composites and PCT/2022/200007 on solvent-base mismatch for the disassembly of epoxy polymers, both submitted by Aarhus University.