

FOLLOWUS
a.State Key Laboratory of Polymer Materials Engineering, College of Polymer Science and Engineerng, Sichuan University, Chengdu 610065, China
b.Guangdong Provincial Key Laboratory of Natural Rubber Processing, Agricultural Products Processing Research Institute of Chinese Academy of Tropical Agricultural Sciences, Zhanjiang 524001, China
276491692@qq.com (L.S.L.)
wujinrong@scu.edu.cn (J.R.W.)
Received:03 April 2021,
Revised:2021-5-13,
Accepted:15 May 2021,
Online First:29 July 2021,
Published:20 August 2021
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Wu, H. T.; Jin, B. Q.; Wang, H.; Wu, W. Q.; Cao, Z. X.; Yuan, Z. Y.; Huang, Y.; Li, W. H.; Huang, G. S.; Liao, L. S.; Wu, J. R. A robust self-healing polyurethane elastomer enabled by tuning the molecular mobility and phase morphology through disulfide bonds. Chinese J. Polym. Sci. 2021, 39, 1299–1309
Hai-Tao Wu, Bi-Qiang Jin, Hao Wang, et al. A Robust Self-healing Polyurethane Elastomer Enabled by Tuning the Molecular Mobility and Phase Morphology through Disulfide Bonds[J]. Chinese Journal of Polymer Science, 2021, 39(10): 1299-1309.
Wu, H. T.; Jin, B. Q.; Wang, H.; Wu, W. Q.; Cao, Z. X.; Yuan, Z. Y.; Huang, Y.; Li, W. H.; Huang, G. S.; Liao, L. S.; Wu, J. R. A robust self-healing polyurethane elastomer enabled by tuning the molecular mobility and phase morphology through disulfide bonds. Chinese J. Polym. Sci. 2021, 39, 1299–1309 DOI: 10.1007/s10118-021-2607-y.
Hai-Tao Wu, Bi-Qiang Jin, Hao Wang, et al. A Robust Self-healing Polyurethane Elastomer Enabled by Tuning the Molecular Mobility and Phase Morphology through Disulfide Bonds[J]. Chinese Journal of Polymer Science, 2021, 39(10): 1299-1309. DOI: 10.1007/s10118-021-2607-y.
Elastomers with outstanding strength
toughness and healing efficiency are highly promising for many emerging fields. However
it is still a challenge to integrate all these beneficial features in one elastomer. Herein
an asymmetric alicyclic structure adjacent to aromatic disulfide was tactfully introduced into the backbone of polyurethane (PU) elastomer. Specifically
such elastomer (PU-HPS) was fabricated by polycondensing polytetramethylene ether glycol (PTMEG)
isophorone diisocyanate (IPDI) and
p
-hydroxydiphenyl disulfide (HPS)
via
one-pot method. The molecular mobility and phase morphology of PU-HPS can be tuned by adjusting the HPS content. Consequently
the dynamic exchange of hydrogen and disulfide bonds in the hard segment domains can also be tailored. The optimized sample manifests outstanding tensile strength (46.4 MPa)
high toughness (109.1 MJ/m
3
)
high self-healing efficiency after fracture (90.3%)
complete scratch recovery (100%) and good puncture resistance. Therefore
this work provides a facile strategy for developing robust self-healing polymers.
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