Isothermal crystallization kinetics in the miscible blend system isota
ctic/atactic poly(P-hydroxybutyrate) (PHB) are examined by optical mic
roscopy. The presence of the atactic component results in a reduction
in spherulitic growth rate of the isotactic polymer. Analysis of the g
rowth rates using the Lauritzen-Hoffman model shows that a regime II -
-> III transition is present for all blend compositions investigated (
0-50 wt% atactic), and that this transition occurs at a constant tempe
rature of 140 degrees C. The ratio of the nucleation constants for the
two regimes, K-g(III)/K-g(II), is found to deviate from the theoretic
al value of 2.0 in the blend system. It is shown that a modified versi
on of the Lauritzen-Hoffman equation incorporating entropic effects is
unable to account for these deviations. The work of chain-folding, q,
is calculated to be 5.1 kcal mol(-1) for isotactic PHB. The implicati
ons of using assumed values of the transport parameters in the kinetic
analysis are discussed.