Self-healing Polyurethane Elastomer Based on Molecular Design: Combination of Reversible Hydrogen Bonds and High Segment Mobility

Author(s):  
Zhaopeng Liang ◽  
Dongao Huang ◽  
Lei Zhao ◽  
Yijing Nie ◽  
Zhiping Zhou ◽  
...  
2020 ◽  
Vol 22 (31) ◽  
pp. 17620-17631
Author(s):  
Xianling Chen ◽  
Jing Zhu ◽  
Yanlong Luo ◽  
Jun Chen ◽  
Xiaofeng Ma ◽  
...  

The changes in the type and number of hydrogen bonds as well as the microscopic behavior of molecular diffusion in the self-healing process of polyurethane are revealed.


2020 ◽  
Vol 44 (15) ◽  
pp. 5746-5754 ◽  
Author(s):  
Xue Wang ◽  
Huijuan Zhang ◽  
Biao Yang ◽  
Liguo Wang ◽  
Hui Sun

A self-healing PU elastomer modulated by disulfide and hydrogen bonding with high transparency of 97% was reported.


2021 ◽  
pp. 110838
Author(s):  
Liyuan Qiao ◽  
Chengde Liu ◽  
Cheng Liu ◽  
Lishuai Zong ◽  
Hongjian Gu ◽  
...  

Polymer ◽  
2020 ◽  
Vol 193 ◽  
pp. 122355
Author(s):  
Shiwen Yang ◽  
Xiaosheng Du ◽  
Zongliang Du ◽  
Mi Zhou ◽  
Xu Cheng ◽  
...  

2020 ◽  
Vol 117 (21) ◽  
pp. 11299-11305 ◽  
Author(s):  
Hao Wang ◽  
Hanchao Liu ◽  
Zhenxing Cao ◽  
Weihang Li ◽  
Xin Huang ◽  
...  

Glassy polymers are extremely difficult to self-heal below their glass transition temperature (Tg) due to the frozen molecules. Here, we fabricate a series of randomly hyperbranched polymers (RHP) with high density of multiple hydrogen bonds, which showTgup to 49 °C and storage modulus up to 2.7 GPa. We reveal that the hyperbranched structure not only allows the external branch units and terminals of the molecules to have a high degree of mobility in the glassy state, but also leads to the coexistence of “free” and associated complementary moieties of hydrogen bonds. The free complementary moieties can exchange with the associated hydrogen bonds, enabling network reconfiguration in the glassy polymer. As a result, the RHP shows amazing instantaneous self-healing with recovered tensile strength up to 5.5 MPa within 1 min, and the self-healing efficiency increases with contacting time at room temperature without the intervention of external stimuli.


2020 ◽  
Vol 8 (44) ◽  
pp. 23330-23343
Author(s):  
Haibin Sun ◽  
Xueying Liu ◽  
Suting Liu ◽  
Bing Yu ◽  
Nanying Ning ◽  
...  

A silicone dielectric elastomer with simultaneous high dielectric constant, fast and efficient self-healing ability at mild conditions was prepared by constructing supramolecular network assembled by coordination bonds and hydrogen bonds.


Polymers ◽  
2020 ◽  
Vol 12 (1) ◽  
pp. 239 ◽  
Author(s):  
Jie Wen ◽  
Xiaopeng Zhang ◽  
Mingwang Pan ◽  
Jinfeng Yuan ◽  
Zhanyu Jia ◽  
...  

Commonly synthetic polyethylene glycol polyurethane (PEG–PU) hydrogels possess poor mechanical properties, such as robustness and toughness, which limits their load-bearing application. Hence, it remains a challenge to prepare PEG–PU hydrogels with excellent mechanical properties. Herein, a novel double-crosslinked (DC) PEG–PU hydrogel was fabricated by combining chemical with physical crosslinking, where trimethylolpropane (TMP) was used as the first chemical crosslinker and polyphenol compound tannic acid (TA) was introduced into the single crosslinked PU network by simple immersion process. The second physical crosslinking was formed by numerous hydrogen bonds between urethane groups of PU and phenol hydroxyl groups in TA, which can endow PEG–PU hydrogel with good mechanical properties, self-recovery and a self-healing capability. The research results indicated that as little as a 30 mg·mL−1 TA solution enhanced the tensile strength and fracture energy of PEG–PU hydrogel from 0.27 to 2.2 MPa, 2.0 to 9.6 KJ·m−2, respectively. Moreover, the DC PEG–PU hydrogel possessed good adhesiveness to diverse substrates because of TA abundant catechol groups. This work shows a simple and versatile method to prepare a multifunctional DC single network PEG–PU hydrogel with excellent mechanical properties, and is expected to facilitate developments in the biomedical field.


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