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Renewable thiol-yne ‘click’ networks based on propargylated lignin for adhesive resin applications

Authors :
Monika A. Jedrzejczyk
Panos D. Kouris
Michael D. Boot
Emiel J.M. Hensen
Katrien V. Bernaerts
AMIBM
RS: FSE AMIBM
Inorganic Materials & Catalysis
Energy Technology
EIRES Chem. for Sustainable Energy Systems
Source :
ACS Applied Polymer Materials, 4(4), 2544-2552. American Chemical Society
Publication Year :
2022
Publisher :
American Chemical Society, 2022.

Abstract

In this study, the development of lignin-based resins for wood adhesion applications was demonstrated. We investigated two lignin fractions: commercial Protobind 1000 lignin and methanol-soluble Protobind 1000 lignin fraction after mild solvolysis. Although lignin has previously been incorporated into various cross-linked systems, this is the first report on lignin-based thermosets obtained via thiol–yne “click” chemistry. In this approach, lignin was functionalized with terminal alkyne groups followed by cross-linking with a multifunctional thiol, resulting in polymeric network formation. The influence of the curing conditions on the resin characteristics and performance was studied, by varying the amount of reactive monomeric diluents. Additionally, a post-curing strategy utilizing the Claisen rearrangement was investigated. These resins were tested as a wood adhesive and were proven to possess a desirable performance, comparable to the state-of-art phenol-formaldehyde resins. Lignin-based thiol–yne resins turn out to be an alternative to phenol-formaldehyde resins, currently used as adhesives and coatings. Although it is possible to use lignin in phenol-formaldehyde resins, lignin addition is compromising the resin’s performance. The main benefits over the phenol-formaldehyde approach are that higher lignin loadings are possible to achieve, and no volatiles are emitted during the resin processing and use.

Details

Language :
English
ISSN :
26376105
Volume :
4
Issue :
4
Database :
OpenAIRE
Journal :
ACS Applied Polymer Materials
Accession number :
edsair.doi.dedup.....ef4414389326eab08411ae9c99c0cbf3