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March 5, 2012Proceedings of the National Academy of Sciences708 citationsOpen Access

Rapid self-healing hydrogels

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APAmeya PhadkeCZChao ZhangBABedri Arman

Key Points

  • To engineer permanently cross-linked hydrogels capable of rapid, autonomous, and reversible self-repair in an aqueous environment.
  • Synthesized permanently cross-linked hydrogel networks functionalized with flexible-pendant side chains containing balanced hydrophilic and hydrophobic moieties.
  • Assessed interfacial self-healing kinetics upon crack introduction, re-attachment capabilities across separate hydrogel fragments, and responsiveness to pH adjustments.
  • Achieved autonomous self-healing within seconds of crack propagation or direct contact between separated hydrogel segments in aqueous conditions.
  • Demonstrated reversible, pH-controlled on-and-off switching of the healing mechanism with preserved mechanical properties and kinetics across multiple damage cycles.

Abstract

Synthetic materials that are capable of autonomous healing upon damage are being developed at a rapid pace because of their many potential applications. Despite these advancements, achieving self-healing in permanently cross-linked hydrogels has remained elusive because of the presence of water and irreversible cross-links. Here, we demonstrate that permanently cross-linked hydrogels can be engineered to exhibit self-healing in an aqueous environment. We achieve this feature by arming the hydrogel network with flexible-pendant side chains carrying an optimal balance of hydrophilic and hydrophobic moieties that allows the side chains to mediate hydrogen bonds across the hydrogel interfaces with minimal steric hindrance and hydrophobic collapse. The self-healing reported here is rapid, occurring within seconds of the insertion of a crack into the hydrogel or juxtaposition of two separate hydrogel pieces. The healing is reversible and can be switched on and off via changes in pH, allowing external control over the healing process. Moreover, the hydrogels can sustain multiple cycles of healing and separation without compromising their mechanical properties and healing kinetics. Beyond revealing how secondary interactions could be harnessed to introduce new functions to chemically cross-linked polymeric systems, we also demonstrate various potential applications of such easy-to-synthesize, smart, self-healing hydrogels.

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Cite This Study

Phadke et al. (2012) studied this question.

synapsesocial.com/papers/69d970491ad561c6736842dfhttps://doi.org/10.1073/pnas.1201122109
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