Renewable Thiol–yne “Click” Networks Based on Propargylated Lignin for Adhesive Resin Applications AITranslate
Abstract AITranslate
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.
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DOI:https://doi.org/10.1021/acsapm.1c01853
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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.
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| GB/T 7714-2015 | [1] Monika A. Jedrzejczyk, Panos D. Kouris, Michael D. Boot, et al. ACS Applied Polymer Materials, 2022(4). DOI:10.1021/acsapm.1c01853. |
| MLA | [1] Monika A. Jedrzejczyk, et al., ACS Applied Polymer Materials, no. 4, 2022, https://doi.org/10.1021/acsapm.1c01853. |
| APA | [1] Monika A. Jedrzejczyk, Panos D. Kouris, Michael D. Boot, Emiel J.M. Hensen, & Katrien V. Bernaerts. (2022). ACS Applied Polymer Materials(4). https://doi.org/10.1021/acsapm.1c01853 |
| IEEE | [1] Monika A. Jedrzejczyk, Panos D. Kouris, Michael D. Boot, Emiel J.M. Hensen, and Katrien V. Bernaerts, ACS Applied Polymer Materials, no. 4, 2022, doi: 10.1021/acsapm.1c01853. keywords: {lignin;propargylated lignin;thiol−yne;“click” chemistry;thermosets;wood adhesives} |
