Chemically induced repair, adhesion, and recycling of polymers made by inverse vulcanization

Samuel J. Tonkin, Christopher T. Gibson, Jonathan A. Campbell, David A. Lewis, Amir Karton, Tom Hasell, Justin M. Chalker

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

Inverse vulcanization is a copolymerization of elemental sulfur and alkenes that provides unique materials with high sulfur content (typically ≥50% sulfur by mass). These polymers contain a dynamic and reactive polysulfide network that creates many opportunities for processing, assembly, and repair that are not possible with traditional plastics, rubbers and thermosets. In this study, we demonstrate that two surfaces of these sulfur polymers can be chemically joined at room temperature through a phosphine or amine-catalyzed exchange of the S-S bonds in the polymer. When the nucleophile is pyridine or triethylamine, we show that S-S metathesis only occurs at room temperature for a sulfur rank > 2—an important discovery for the design of polymers made by inverse vulcanization. This mechanistic understanding of the S-S metathesis was further supported with small molecule crossover experiments in addition to computational studies. Applications of this chemistry in latent adhesives, additive manufacturing, polymer repair, and recycling are also presented.

Original languageEnglish
Pages (from-to)5537-5546
Number of pages10
JournalChemical Science
Volume11
Issue number21
DOIs
Publication statusPublished - 7 Jun 2020

Bibliographical note

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. All publication charges for this article have been paid for by the Royal Society of Chemistry.

Keywords

  • Inverse vulcanization
  • polymers
  • polysulfide
  • adhesives
  • recycling

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