One-Step Soaking Strategy toward Anti-Swelling Hydrogels with a Stiff Armor

Double-network (DN) hydrogels consisting of noncovalent interacting networks are highly desired due to their well-controlled compositions and environmental friendliness, but the low water resistance always impairs their mechanical strength. Here, an anti-swelling hydrogel possessing the core/shell architecture through rational regulation of multiple weak noncovalent interactions is prepared. A composite hydrogel consists of chitosan (CS) and poly(N-acryloyl 2-glycine) (PACG), readily forming the shell-structured DN hydrogel after soaking in a FeCl3 solution because of in situ formation of chain entanglements, hydrogen bonds, and ionic coordination. The produced DN hydrogels exhibit excellent anti-swelling behaviors and mechanical durability for over half a year, even in some strict situations. Taking the merits of noncovalent bonds in adjustability and reversibility, the swelling property of these hydrogels can be easily customized through control of the ion species and concentrations. A dynamically reversible transition from super-swelling to anti-swelling is realized by breaking up and rebuilding the metal-coordination complexes. This facile but efficient strategy of turning the noncovalent interactions and consequently the mechanics and anti-swelling properties is imperative to achieve the rational design of high-performance hydrogels with specific usage requirements and expand their applicability to a higher stage.

Automated summary

A novel hydrogel with a core/shell structure is prepared through rational regulation of weak noncovalent interactions. The hydrogel exhibits excellent anti-swelling behaviors and mechanical durability due to the formation of chain entanglements, hydrogen bonds, and ionic coordination. The swelling property of the hydrogel can be easily customized by controlling the ion species and concentrations, and a reversible transition from super-swelling to anti-swelling is achieved by breaking up and rebuilding metal-coordination complexes.