Synergistic Dual Dynamic Covalent Networks Enable High-Performance and Self-Healing Polyurethane and Its Anticorrosion Applications

Intrinsic self-healing polymers have gained significant attention due to their potential to extend material lifespan and enhance sustainability. However, balancing mechanical strength and self-healing performance remains a challenge for self-healing polymers. This study presents a dual dynamic covalent bond strategy by incorporating two chain extenders, 2,5-bis(4-hydroxyphenyl) disulfide (BHPS) and furandimethanol (FDME), into the polyurethane structure. A cross-linked network was formed via the Diels–Alder reaction between FDME and bismaleimide (BMI), which worked synergistically with dynamic disulfide bonds to effectively address the challenge. When the molar ratio of BHPS to FDME was 1:1, the material exhibited a tensile strength of 31 MPa, toughness of 97 MJ·m–3, outstanding self-healing capability at 100 °C, and multiple recyclability. Electrochemical tests demonstrated its potential as a self-healing anticorrosion coating. This molecular design strategy effectively addresses the challenge of balancing mechanical performance and self-healing efficiency in polymers, providing a new approach for sustainable functional materials.

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Publication Details

Journal
Macromolecules
Published
2025-07-16
DOI
https://doi.org/10.1021/acs.macromol.5c01097
Citations
5
Primary Topic
Polymer composites and self-healing
Type
article
Field-Weighted Citation Impact
3.03

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article

Synergistic Dual Dynamic Covalent Networks Enable High-Performance and Self-Healing Polyurethane and Its Anticorrosion Applications

Liang Yu, Wuxiang Chen, Kaifeng Chen, Yanhui Cao et al.
5 citations
Macromolecules
Polymer composites and self-healing
3.03
article

Synergistic Dual Dynamic Covalent Networks Enable High-Performance and Self-Healing Polyurethane and Its Anticorrosion Applications

Liang Yu, Wuxiang Chen, Kaifeng Chen, Yanhui Cao, Miaoming Huang, Zhibin Wang, Jingjing Wang, Yan Le, Wenhua Chen, Suqin He, Wentao Liu, Yuqing Wang, J. R. Mao
article en
5 citations

Abstract

Intrinsic self-healing polymers have gained significant attention due to their potential to extend material lifespan and enhance sustainability. However, balancing mechanical strength and self-healing performance remains a challenge for self-healing polymers. This study presents a dual dynamic covalent bond strategy by incorporating two chain extenders, 2,5-bis(4-hydroxyphenyl) disulfide (BHPS) and furandimethanol (FDME), into the polyurethane structure. A cross-linked network was formed via the Diels–Alder reaction between FDME and bismaleimide (BMI), which worked synergistically with dynamic disulfide bonds to effectively address the challenge. When the molar ratio of BHPS to FDME was 1:1, the material exhibited a tensile strength of 31 MPa, toughness of 97 MJ·m–3, outstanding self-healing capability at 100 °C, and multiple recyclability. Electrochemical tests demonstrated its potential as a self-healing anticorrosion coating. This molecular design strategy effectively addresses the challenge of balancing mechanical performance and self-healing efficiency in polymers, providing a new approach for sustainable functional materials.

MacromoleculesVol. 58(15)
Huaqiao University (CN), Zhengzhou University (CN), Shanghai Shipbuilding Technology Research Institute (CN), Division of Materials Science and Engineering (AU), Marine Design & Research Institute of China (CN), China State Shipbuilding (China) (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 8%
Polymer composites and self-healing
3.03
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