A Waterborne Epoxy Vitrimer: Enabling Moisture‐Driven Actuation, Continuous Moist‐Electric Generation, and Water‐Assisted Degradation

The integration of multiple hydroxyl structures presents a robust strategy for designing epoxy vitrimers based on transesterification reactions (TERs), enabling the realization of optimal dynamic properties. Nevertheless, significant challenges persist in achieving eco-friendly synthesis, hydrophilic-related functionalities, and sustainable degradation. Here, a catalyst-free waterborne epoxy vitrimer is developed by curing 1,4-butanediol diglycidyl ether with natural L-tartaric acid (L-TA), effectively addressing these challenges simultaneously. Harnessing the synergistic effects of multiple hydroxyl groups and the neighboring group participation effect imparted by L-TA, the resulting vitrimer exhibits rapid stress relaxation (τ<sup>*</sup> = 270 s at 190 °C) and undergoes complete degradation in 95 °C pure water within 6 h. Furthermore, the abundant hydroxyl groups on polymer chains facilitate its function as a moisture-responsive actuator, achieving a crimping speed of 0.32 mm s<sup>-1</sup>. Building on this, a moist-electric generator is engineered by utilizing the vitrimer as a matrix for ambient vapor collection and subsequent conversion into electrical energy. This device sustains a stable voltage output (0.42-0.50 V) under ambient conditions for 60 h, with capabilities for series amplification and capacitor charging. This study maximizes the potential of hydroxyl-rich TERs-based epoxy vitrimers, paving the way for the advancement and practical implementation of sustainable polymers.

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Publication Details

Journal
Advanced Science
Published
2025-10-08
DOI
https://doi.org/10.1002/advs.202513579
Citations
4
Primary Topic
Polymer composites and self-healing
Type
article
Field-Weighted Citation Impact
2.43

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article

A Waterborne Epoxy Vitrimer: Enabling Moisture‐Driven Actuation, Continuous Moist‐Electric Generation, and Water‐Assisted Degradation

Jianhua Tang, Ousheng Zhang, Dongxu Pei, Jianqiao Wu et al.
4 citations
Advanced Science
Polymer composites and self-healing
2.43
article

A Waterborne Epoxy Vitrimer: Enabling Moisture‐Driven Actuation, Continuous Moist‐Electric Generation, and Water‐Assisted Degradation

Jianhua Tang, Ousheng Zhang, Dongxu Pei, Jianqiao Wu, Zixuan Wang, Qiuyang Ma, Yan Zhang, Jun Hu, Yaning Ma
article en
4 citations

Abstract

The integration of multiple hydroxyl structures presents a robust strategy for designing epoxy vitrimers based on transesterification reactions (TERs), enabling the realization of optimal dynamic properties. Nevertheless, significant challenges persist in achieving eco-friendly synthesis, hydrophilic-related functionalities, and sustainable degradation. Here, a catalyst-free waterborne epoxy vitrimer is developed by curing 1,4-butanediol diglycidyl ether with natural L-tartaric acid (L-TA), effectively addressing these challenges simultaneously. Harnessing the synergistic effects of multiple hydroxyl groups and the neighboring group participation effect imparted by L-TA, the resulting vitrimer exhibits rapid stress relaxation (τ<sup>*</sup> = 270 s at 190 °C) and undergoes complete degradation in 95 °C pure water within 6 h. Furthermore, the abundant hydroxyl groups on polymer chains facilitate its function as a moisture-responsive actuator, achieving a crimping speed of 0.32 mm s<sup>-1</sup>. Building on this, a moist-electric generator is engineered by utilizing the vitrimer as a matrix for ambient vapor collection and subsequent conversion into electrical energy. This device sustains a stable voltage output (0.42-0.50 V) under ambient conditions for 60 h, with capabilities for series amplification and capacitor charging. This study maximizes the potential of hydroxyl-rich TERs-based epoxy vitrimers, paving the way for the advancement and practical implementation of sustainable polymers.

Advanced ScienceVol. 13(2)
Sinopec (China) (CN), Chuzhou University (CN), Beijing University of Chemical Technology (CN)
National Natural Science Foundation of China, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 11%
Polymer composites and self-healing
2.43
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