Poor toughness and fast hydrolysis
degradation are the
key barriers
for poly(glycolic acid) (PGA) toward broader applications. Herein,
nonlinear structure PGA with high toughness and excellent hydrolysis
stability was prepared through graft and chain extending reaction
in the presence of bis(tert-butylperoxyisopropyl)benzene
(BIPB) and glycidyl methacrylate (GMA). The rheological behavior,
the gel content, and the GPC result demonstrated that GMA was grafted
onto PGA chains, and then the epoxy group of grafted GMA reacted with
the end groups of PGA, which resulted in the formation of a nonlinear
structure in which one original PGA chain connected to the other PGA
backbone. The PGA/1.0BIPB/1.0GMA which had the highest nonlinear degree
was obtained when the amounts of BIPB and GMA were all 1.0 wt % with
respect to PGA, and it showed some excellent characterization. Compared
to that of virgin PGA, the elongation at break and impact strength
of PGA/1.0BIPB/1.0GMA increased by 547 and 18%, respectively. Moreover,
PGA/1.0BIPB/1.0GMA also possessed a faster crystallization rate. The
hydrolysis results showed that the tensile strength of PGA/1.0BIPB/1.0GMA
decreased by half on the 12th day, delaying by 7 days compared with
that of virgin PGA. Furthermore, PGA/1.0BIPB/1.0GMA also had better
foaming ability of a 24.68-fold volume expansion ratio. Thus, this
work paved a new strategy to design nonlinear structure PGA with high
toughness, excellent hydrolysis stability, and ultrahigh foamability.