A facile
strategy was developed for the formation of an autonomous
chitosan-based self-healing hydrogel. This hydrogel was fabricated
using in situ free radical polymerization of acrylic
acid (AA) and acrylamide (AM) in the presence of chitosan in dilute
acetic acid aqueous solution under mild conditions. The in
situ formed hydrogel is mainly composed of chitosan graft
copolymers (CS-g-P(AM-r-AA)) and
a small amount of nongrafted copolymers (P(AM-r-AA)),
which interact with each other through a combination of multiple noncovalent
interactions, including the interchain electrostatic complexation
between −[AA]– segments and positively charged amino
groups of chitosan, the H-bonding between −[AM]– segments,
and the H-bonding between −[AM]– segments and the chitosan
backbone. Owing to the cooperation of these noncovalent interactions
and the reversible nature of the noncovalent network structure, the
obtained hydrogel exhibits rapid network recovery, high stretchability,
and efficient autonomous self-healing properties. The hydrogel can
also dissolve completely in dilute acidic aqueous solution under mild
conditions, visibly reflecting the unique network feature of this
self-healing hydrogel system