High-strength and self-healing bio-based polyhydroxyurethanes for high-temperature adhesives
New research shows promising properties of bio-based PHUs as high-performance adhesives.

Polyhydroxyurethanes (PHUs) are considered a sustainable and safe alternative to traditional isocyanate-based polyurethanes (PUs). A recent study shows that a strong and rapidly self-healing bio-based PHU network has been developed based on carbonated daidzein (DZ-BCC) and amines.
The use of amino-propyl-terminated polydimethylsiloxane (H2N-PDMS-NH2) as a soft segment increases chain mobility and thus optimises the self-healing properties. At the same time, the high crosslinking density of the network together with the benzopyran ring structure of the daidzein ensures an impressive mechanical strength of up to 28.3 MPa.
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Rapid self-healing and high temperature resistance
Despite this high mechanical stability, the materials show remarkable self-healing: after only 30 minutes at 150 °C, 94% of the original tensile strength can be restored. In addition, these PHU-based materials can be used as adhesives for wood and glass bonding, with shear strengths of up to 6.4 MPa and 3.4 MPa, respectively.
Another advantage is their temperature resistance: bonded glass samples remain stable even at 150 °C. Chemical recyclability and high reprocessability also make these materials particularly attractive for sustainable applications.
Conclusion
The daidzein-based PHUs presented combine high strength with rapid self-healing, thus expanding the range of applications for sustainable high-performance adhesives. Their special properties could create new possibilities for high-temperature bonding in the wood and glass industries.
Source: Jie Liu et al., Polymer Chemistry, Issue 7, 2025.