TY - JOUR
T1 - Fabrication and Performance of Bicontinuous Self-Healing Water-Absorbing and -Swelling Elastomers through Multiscale Synergistic Strategies
AU - Wang, Runhua
AU - Zhu, Yiyao
AU - Wang, Jincheng
AU - Lu, Wentong
AU - Lu, Yue
AU - Liu, Hui
AU - Li, Xiang
AU - Zhang, Hua
N1 - Publisher Copyright:
© 2025 American Chemical Society
PY - 2025/12/26
Y1 - 2025/12/26
N2 - 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.
AB - 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.
KW - dynamic reversible covalent bond
KW - multiscale
KW - polyurethane
KW - self-healing
KW - water-absorbing and expansion
UR - https://www.scopus.com/pages/publications/105025701409
U2 - 10.1021/acsapm.5c03337
DO - 10.1021/acsapm.5c03337
M3 - 文章
AN - SCOPUS:105025701409
SN - 2637-6105
VL - 7
SP - 16649
EP - 16660
JO - ACS Applied Polymer Materials
JF - ACS Applied Polymer Materials
IS - 24
ER -