Poly(3-hydroxybutyrate) (PHB) and its copolymer poly(3-hydroxybutyrate
-3-hydroxyvalerate) [P(HB-HV)] were irradiated with gamma-rays in air
or vacuum. Polymer chain scission occurred and resulted in depression
of melting points (T-m), glass-transition temperatures (T-g) and numbe
r-average molecular weight (($) over bar M(n)). Decrease in ($) over b
ar M(n) of the sample irradiated in vacuum was smaller than that irrad
iated in air, implying introduction of crosslinking. The T-m and T-g o
f samples irradiated in air were inversely proportional to ($) over ba
r M(n). Their biodegradability was clearly promoted with decreasing ($
) over bar M(n). Radiation grafting of methyl methacrylate (MMA) or 2-
hydroxyethyl methacrylate (HEMA) was carried out by in-source polymeri
zation. Degree of grafting (X(g)) increased as irradiation dose increa
sed and leveled off around 5 kGy. The X(g) of PHB grafted was lower th
an that of P(HB-HV) because of higher crystallinity of the former. Cro
sslinking between the grafted PMMA chains was easily formed. Biodegrad
ability of both polymers steeply decreased by introduction of MMA graf
ting, while that of polymers grafted with HEMA increased at first beca
use of improvement of wetiability then steeply decreased with increasi
ng X(g) of HEMA.