Jia, X. T.; Sun, Y. T.; Ni, C. J.; Zhao, Q. Enhanced mechanical properties and prolonged recovery onset period of timed shape memory hydrogels via hydrophobic interaction. Chinese J. Polym. Sci. 2026, 44, 2043–2050
Xiao-Ting Jia, Yi-Ting Sun, Chu-Jun Ni, et al. Enhanced Mechanical Properties and Prolonged Recovery Onset Period of Timed Shape Memory Hydrogels via Hydrophobic Interaction[J]. Chinese Journal of Polymer Science, 2026, 44(7): 2043-2050. DOI: 10.1007/s10118-026-3666-x.
Jia, X. T.; Sun, Y. T.; Ni, C. J.; Zhao, Q. Enhanced mechanical properties and prolonged recovery onset period of timed shape memory hydrogels via hydrophobic interaction. Chinese J. Polym. Sci. 2026, 44, 2043–2050DOI: 10.1007/s10118-026-3666-x.
Xiao-Ting Jia, Yi-Ting Sun, Chu-Jun Ni, et al. Enhanced Mechanical Properties and Prolonged Recovery Onset Period of Timed Shape Memory Hydrogels via Hydrophobic Interaction[J]. Chinese Journal of Polymer Science, 2026, 44(7): 2043-2050. DOI: 10.1007/s10118-026-3666-x.DOI:
Enhanced Mechanical Properties and Prolonged Recovery Onset Period of Timed Shape Memory Hydrogels via Hydrophobic Interaction
Acrylates with varied hydrophobic chains are copolymerized with acrylic acid to fabricate timed shape memory hydrogels
providing superior mechanical properties and an extremely long recovery onset period.
Abstract
Shape memory behavior with programmable recovery onset have been discovered very recently in poly(acrylic acid) hydrogels crosslinked by calcium ions. Their ability to undergo apparent autonomous and timed shape transformation
governed by thermal-sensitive phase evolution
has attracted growing interests particularly for the development of trigger-free biomedical devices. While copolymerization with various monomers can introduce multifunctional properties
this strategy often compromises the phase-separated microstructure and shortens the recovery onset period. Here we introduce hydrophobic acrylate comonomers with different lengths of aliphatic chains to investigate various properties of the copolymerized hydrogels. Upon the same comonomer weight percentage of 20 wt%
short alkyl chains disrupt the polymer aggregation and disable the timed recovery. In contrast
longer alkyl chains form hydrophobic domains which enhance the mechanical properties of the hydrogel and prolong the onset time. Quantitatively
the copolymer hydrogel provided excellent tensile strength of 5.25 MPa and maximum onset period of strikingly 800 min
which are respectively 16.7 and 35 times than the homopolymer hydrogel. This work advances the understanding of the hydrogel system with programmable recovery onset and provides a promising molecular modulation strategy for functionalization of hydrogels with responsive phase separation behavior.
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