Highly stretchable, self-healing, and 3D printing prefabricatable hydrophobic association hydrogels with the assistance of electrostatic interaction

Outstanding mechanical performances and designable architectures are essential for hydrogels when applied as structural materials. In this work, a series of physically cross-linked hydrogels were prepared by copolymerization of a hydrophobic monomer of butyl acrylate and an ampholytic cross-linker o...

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Published inPolymer chemistry Vol. 11; no. 29; pp. 4741 - 4748
Main Authors Chen, Heng, Hao, Beibei, Ge, Penghui, Chen, Shaojun
Format Journal Article
LanguageEnglish
Published Cambridge Royal Society of Chemistry 07.08.2020
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Summary:Outstanding mechanical performances and designable architectures are essential for hydrogels when applied as structural materials. In this work, a series of physically cross-linked hydrogels were prepared by copolymerization of a hydrophobic monomer of butyl acrylate and an ampholytic cross-linker of 2-(dimethylamino)ethyl methacrylate and methacrylic acid, followed by soaking in water. The ampholytic cross-linker supported the 3D-printing fabrication of hydrogel precursors, and further hydrated to induce hydrophobic association and caused the transformation from hydrogel precursors to hydrogels. These hydrogels with a water content of 10.4-57.0 wt% possessed excellent mechanical properties, with a tensile strength, elongation at break, and Young's modulus of 61.0-103.4 kPa, 1150-1560%, and 42.7-125.7 kPa, respectively, and meanwhile exhibited fast and high autonomous self-healing ability. This work developed a facile strategy to prepare self-healing hydrophobic association hydrogels besides emulsion polymerization, and offer new ways to construct physically cross-linked hydrogels with designable architectures. Self-healing and 3D printing prefabricatable physically crosslinked hydrogels were prepared by copolymerization of butyl acrylate, 2-(dimethylamino)ethyl methacrylate, and methacrylic acid, followed by soaking in water.
Bibliography:10.1039/d0py00003e
Electronic supplementary information (ESI) available. See DOI
ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:1759-9954
1759-9962
DOI:10.1039/d0py00003e