Abstract

Inverse vulcanization has emerged as a popular strategy for transforming the waste material, elemental sulfur, into functional polymers with high sulfur content (>50 wt.%, normally). Inverse vulcanized polymers are intrinsically processable and recyclable, and have been demonstrated as promising for applications in many fields. However, the mechanical properties of inverse vulcanized polymers are currently underdeveloped. If this kind of material is to be widely used in some scenarios to replace some traditional plastics, it is necessary to make them with appropriate thermal and mechanical properties that meet basic application requirements. Here, we report a series of terpolymers copolymerized from two distinct organic comonomers and elemental sulfur to obtain polymers with a wide range of glass transition temperatures (−43 °C to 45 °C) that exhibit good mechanical properties, by blending crosslinkers with varying feed monomer ratio and chain length of linear sections, which expands the application opportunities of inverse vulcanization.

The thermal and mechanical properties of inverse vulcanized polymers are currently underdeveloped. Here, a series of terpolymers copolymerized from two distinct organic comonomers and elemental sulfur yield polymers with a wide range of glass transition temperatures and show good mechanical properties.

Details

Title
Processable crosslinked terpolymers made from elemental sulfur with wide range of thermal and mechanical properties
Author
Yan, Peiyao 1   VIAFID ORCID Logo  ; Wang, Haoran 1 ; Dodd, Liam James 1 ; Hasell, Tom 1 

 University of Liverpool, Department of Chemistry, Liverpool, UK (GRID:grid.10025.36) (ISNI:0000 0004 1936 8470) 
Pages
89
Publication year
2023
Publication date
Dec 2023
Publisher
Nature Publishing Group
e-ISSN
26624443
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2884938043
Copyright
© The Author(s) 2023. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.