Fabrication and Performance of Bicontinuous Self-Healing Water-Absorbing and -Swelling Elastomers through Multiscale Synergistic Strategies

Water-absorbing expansion elastomers, valuable in environmental engineering, are limited by their low mechanical strength, poor self-healing capacity, and recycling challenges. While polyurethane (PU) offers superior mechanical robustness and weather resistance, it inherently lacks hydrophilicity. To address these gaps, this study developed self-healing, hydrophilic swelling PU elastomers via a multiscale synergistic strategy; rigid crystalline hard segments (imidazolidinyl urea) were integrated with soft segments poly(tetrahydrofuran) glycol and hydrophilic poly(ethylene glycol), and 2-hydroxyethyl disulfide (HEDS) was introduced to modulate interfacial interactions, forming a bicontinuous phase network. Fourier transform infrared spectroscopy confirmed the complete reaction of isocyanate groups, validating successful synthesis. Optical transmittance increased with poly(tetrahydrofuran) glycol (PTMEG) content, while X-ray diffraction revealed an enhanced amorphous phase intensity. Mechanically, polyurethane elastomer (PU2) achieved a toughness of 36.50 MJ/m3, and polyurethane elastomer (PU2–17%) demonstrated a tensile strength of 7.4 MPa with 731% elongation. Self-healing efficiency reached 96% (at 100 °C/6 h) with optimized disulfide bond density, though excessive HEDS slowed thermal response via dynamic bond exchange. Notably, polyurethane elastomer (PU1), containing higher PEG content, exhibited the highest swelling ratio (195% at 24 h). The hygroscopic conductive sensor sample with a sandwich structure, denoted as PU2–17%-PPy, possesses a high humidity responsiveness. Response and recovery tests indicated that it featured a humidity response time of 7 s and a full recovery time of 60 s, which was significantly faster than that of traditional humidity-sensitive materials. By synergizing dynamic bonds, soft segment design, and crystalline hard domains, this work provides a sustainable strategy for advanced functional materials, balancing mechanical durability, environmental responsiveness, and recyclability.

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Publication Details

Journal
ACS Applied Polymer Materials
Published
2025-12-08
DOI
https://doi.org/10.1021/acsapm.5c03337
Primary Topic
Polymer composites and self-healing
Type
article
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article

Fabrication and Performance of Bicontinuous Self-Healing Water-Absorbing and -Swelling Elastomers through Multiscale Synergistic Strategies

ACS Applied Polymer Materials
Polymer composites and self-healing
article

Fabrication and Performance of Bicontinuous Self-Healing Water-Absorbing and -Swelling Elastomers through Multiscale Synergistic Strategies

article en

Abstract

Water-absorbing expansion elastomers, valuable in environmental engineering, are limited by their low mechanical strength, poor self-healing capacity, and recycling challenges. While polyurethane (PU) offers superior mechanical robustness and weather resistance, it inherently lacks hydrophilicity. To address these gaps, this study developed self-healing, hydrophilic swelling PU elastomers via a multiscale synergistic strategy; rigid crystalline hard segments (imidazolidinyl urea) were integrated with soft segments poly(tetrahydrofuran) glycol and hydrophilic poly(ethylene glycol), and 2-hydroxyethyl disulfide (HEDS) was introduced to modulate interfacial interactions, forming a bicontinuous phase network. Fourier transform infrared spectroscopy confirmed the complete reaction of isocyanate groups, validating successful synthesis. Optical transmittance increased with poly(tetrahydrofuran) glycol (PTMEG) content, while X-ray diffraction revealed an enhanced amorphous phase intensity. Mechanically, polyurethane elastomer (PU2) achieved a toughness of 36.50 MJ/m3, and polyurethane elastomer (PU2–17%) demonstrated a tensile strength of 7.4 MPa with 731% elongation. Self-healing efficiency reached 96% (at 100 °C/6 h) with optimized disulfide bond density, though excessive HEDS slowed thermal response via dynamic bond exchange. Notably, polyurethane elastomer (PU1), containing higher PEG content, exhibited the highest swelling ratio (195% at 24 h). The hygroscopic conductive sensor sample with a sandwich structure, denoted as PU2–17%-PPy, possesses a high humidity responsiveness. Response and recovery tests indicated that it featured a humidity response time of 7 s and a full recovery time of 60 s, which was significantly faster than that of traditional humidity-sensitive materials. By synergizing dynamic bonds, soft segment design, and crystalline hard domains, this work provides a sustainable strategy for advanced functional materials, balancing mechanical durability, environmental responsiveness, and recyclability.

ACS Applied Polymer MaterialsVol. 7(24)
University of Science and Technology (YE), Shanghai University of Engineering Science (CN), Ingenierie des Materiaux polymeres (FR)
Openalex Percentile: Top 54%
Polymer composites and self-healing
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