A synchrotron SAXS study of miscible blends of semicrystalline poly(vinylidenefluoride) and semicrystalline poly(1,4-butylene adipate). II. Crystallization, morphology, and PBA inclusion in PVF2 spherulites
Lz. Liu et al., A synchrotron SAXS study of miscible blends of semicrystalline poly(vinylidenefluoride) and semicrystalline poly(1,4-butylene adipate). II. Crystallization, morphology, and PBA inclusion in PVF2 spherulites, J POL SC PP, 38(17), 2000, pp. 2296-2308
The incorporation of poly(1,4-butylene adipate) (PBA) and its crystallizati
on behavior within poly(vinylidenefluoride) (PVF2) spherulites in miscible
PVF2/PBA blends have been further studied with small-angle X-ray synchrotro
n scattering (SAXS). The incorporation of PBA into the PVF2 interlamellar r
egion was found to be dependent on the PVF2 crystallization conditions. In
our previous work, where the blends were crystallized by a one-step quenchi
ng process directly from 190 (a single-phase region) to 20 degrees C (a thr
ee-phase region), the transition from PBA inclusion in the PVF2 interlamell
ar region to interlamellar exclusion occurred at a PBA weight fraction of s
imilar to 0.5. In this case, where the blends were first quenched from 190
(a single-phase region) to 130 degrees C (a two-phase region) and then furt
her quenched to 20 degrees C (a three-phase region), the transition occurre
d at a PBA weight fraction of less than 0.3. That is, when a blend is cryst
allized under different conditions, different amounts of the PBA component
are incorporated into the PVF2 interlamellar phase. The thickness of the PV
F2 interlamellar phase, in turn, may affect the PBA crystalline structure i
n the interlamellar region. Time-resolved SAXS was used to probe the crysta
llization dynamics of both PVF2 and PBA components in a blend containing 60
wt % PBA. The blend was quenched from the single-phase region at 190 to 13
0 degrees C to crystallize the PVF2 component and was then further quenched
to 20 degrees C to crystallize the PBA component. This study, together wit
h our earlier results, shows that the time dependence of the PVF2 crystalli
zation rate and crystalline lamellar thickness is a function of the PBA con
tent in the blend. The glass-transition temperature of the blend and the PB
A diffusion process are the two dominant factors that control the PVF2 crys
tallization dynamics. (C) 2000 John Wiley & Sons, Inc.