Solid–Liquid-Hysteresis Materials Based on Reversible Covalent Cross-Linking of Liquid Monomers

When a two-component liquid resin is cured, it usually ends up in the solid state and cannot be transferred to the liquid state again. This work introduces a polymeric material, which cross-links covalently at ambient temperatures, but can still be liquefied again on demand. The mechanism is based on the well-known concept of reversible cross-links, e.g., via Diels-Alder-reactions, which allow de-cross-linking at elevated temperatures. The presented material, however, differs from known variants by the fact that the non-cross-linked state is liquid at ambient conditions. Thus, the cross-linked solid material can be reversibly transferred to the liquid state again by heating. In contrast to classical melting, the material remains in the liquid state after cooling for a prolonged time. It therefore shows a behavior that is reminiscent of a melting hysteresis but is rather based on a superposition of thermodynamics and kinetics. At room temperature, cross-linking occurs rather slowly, while it is massively accelerated at raised temperatures. In contrast to supercooled liquids with a physical melting hysteresis, materials with a herein described "chemical liquefication hysteresis" are attractive for multiple applications, e.g., recycling, adhesives, coatings, or even polymeric bulk materials.

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Publication Details

Journal
ACS Polymers Au
Published
2025-12-09
DOI
https://doi.org/10.1021/acspolymersau.5c00139
Citations
1
Primary Topic
Polymer composites and self-healing
Type
article
Field-Weighted Citation Impact
0.61
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article

Solid–Liquid-Hysteresis Materials Based on Reversible Covalent Cross-Linking of Liquid Monomers

1 citations
ACS Polymers Au
Polymer composites and self-healing
0.61
article

Solid–Liquid-Hysteresis Materials Based on Reversible Covalent Cross-Linking of Liquid Monomers

article en
1 citations

Abstract

When a two-component liquid resin is cured, it usually ends up in the solid state and cannot be transferred to the liquid state again. This work introduces a polymeric material, which cross-links covalently at ambient temperatures, but can still be liquefied again on demand. The mechanism is based on the well-known concept of reversible cross-links, e.g., via Diels-Alder-reactions, which allow de-cross-linking at elevated temperatures. The presented material, however, differs from known variants by the fact that the non-cross-linked state is liquid at ambient conditions. Thus, the cross-linked solid material can be reversibly transferred to the liquid state again by heating. In contrast to classical melting, the material remains in the liquid state after cooling for a prolonged time. It therefore shows a behavior that is reminiscent of a melting hysteresis but is rather based on a superposition of thermodynamics and kinetics. At room temperature, cross-linking occurs rather slowly, while it is massively accelerated at raised temperatures. In contrast to supercooled liquids with a physical melting hysteresis, materials with a herein described "chemical liquefication hysteresis" are attractive for multiple applications, e.g., recycling, adhesives, coatings, or even polymeric bulk materials.

ACS Polymers AuVol. 6(1)
Universität Innsbruck (AT), H.C. Starck (Germany) (DE)
Openalex Percentile: Top 27%
Polymer composites and self-healing
0.61
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