Engineered Functional Segments Enabled Mechanically Robust, Intrinsically Fire‐Retardant, Switchable, Degradable PolyureThane Adhesives

Abstract Adhesives are being used ubiquitously, such as automotive, building, electronics, and beyond. Due to the lack of rational design strategies, they have yet to achieve a performance portfolio: mechanically robust, highly adhesive, fire‐retardant, switchable, and sustainable (e.g., biobased, reusable, biodegradable) to ensure their practical applications. Herein, a fire‐retardant phosphorus‐containing pimaric acid bio‐derivative, AD, as functional segments, is rationally engineered to prepare biobased polyurethane (PU) adhesive that realizes such an integrated performance portfolio. Because of dynamic hydrogen‐bonding and π–π stacking of polar AD, the as‐prepared PU adhesive exhibits an ultrahigh adhesion force of 38.8 N cm –1 . As‐prepared adhesive can be readily reused benefiting from its good solubility in ethanol and exhibits temperature‐responsive switchable adhesion without degraded adhesion. Also, the adhesive shows intrinsic fire retardance due to its biphasic modes of action. The labile ester bonds in the structure enable the adhesive to completely degrade in the presence of lipase or dilute acid. Further demonstration of its promising applications as an adhesive for nanocomposite heat dissipators shows superior dissipating efficiencies to commercial heat sinks. This work offers a novel design approach for creating next‐generation sustainable high‐performance adhesives with functional integration and circular life cycles, which are anticipated to find extensive real‐world applications.

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Institutions

Publication Details

Journal
Advanced Functional Materials
Published
2024-09-05
DOI
https://doi.org/10.1002/adfm.202409139
Citations
58
Primary Topic
Polymer composites and self-healing
Type
article
Field-Weighted Citation Impact
9.78

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article

Engineered Functional Segments Enabled Mechanically Robust, Intrinsically Fire‐Retardant, Switchable, Degradable PolyureThane Adhesives

Bryan T. Tuten, Siqi Huo, Ziqi Sun, Pingan Song et al.
58 citations
Advanced Functional Materials
Polymer composites and self-healing
9.78
article

Engineered Functional Segments Enabled Mechanically Robust, Intrinsically Fire‐Retardant, Switchable, Degradable PolyureThane Adhesives

Bryan T. Tuten, Siqi Huo, Ziqi Sun, Pingan Song, Mark Lynch, Yijiao Xue, Meng Zhang, Wei Zheng, Zhewen Ma, Yonghong Zhou
article en
58 citations

Abstract

Abstract Adhesives are being used ubiquitously, such as automotive, building, electronics, and beyond. Due to the lack of rational design strategies, they have yet to achieve a performance portfolio: mechanically robust, highly adhesive, fire‐retardant, switchable, and sustainable (e.g., biobased, reusable, biodegradable) to ensure their practical applications. Herein, a fire‐retardant phosphorus‐containing pimaric acid bio‐derivative, AD, as functional segments, is rationally engineered to prepare biobased polyurethane (PU) adhesive that realizes such an integrated performance portfolio. Because of dynamic hydrogen‐bonding and π–π stacking of polar AD, the as‐prepared PU adhesive exhibits an ultrahigh adhesion force of 38.8 N cm –1 . As‐prepared adhesive can be readily reused benefiting from its good solubility in ethanol and exhibits temperature‐responsive switchable adhesion without degraded adhesion. Also, the adhesive shows intrinsic fire retardance due to its biphasic modes of action. The labile ester bonds in the structure enable the adhesive to completely degrade in the presence of lipase or dilute acid. Further demonstration of its promising applications as an adhesive for nanocomposite heat dissipators shows superior dissipating efficiencies to commercial heat sinks. This work offers a novel design approach for creating next‐generation sustainable high‐performance adhesives with functional integration and circular life cycles, which are anticipated to find extensive real‐world applications.

Advanced Functional MaterialsVol. 34(49)
Tongji University (CN), Queensland University of Technology (AU), University of Southern Queensland (AU), Institute of Chemical Industry of Forest Products (CN), Chinese Academy of Forestry (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Australian Research Council
Openalex Percentile: Top 1%
Polymer composites and self-healing
9.78
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