ACTIVATION-ENERGY FOR CRYSTALLIZATION OF LOW-MOLECULAR-WEIGHT POLY(ETHYLENE OXIDE) AND LOW-MOLECULAR-WEIGHT POLY(ETHYLENE OXIDE) POLY(METHYL METHACRYLATE) BLENDS DETERMINED BY DSC AND POLARIZED OPTICAL MICROSCOPY/
S. Imai et al., ACTIVATION-ENERGY FOR CRYSTALLIZATION OF LOW-MOLECULAR-WEIGHT POLY(ETHYLENE OXIDE) AND LOW-MOLECULAR-WEIGHT POLY(ETHYLENE OXIDE) POLY(METHYL METHACRYLATE) BLENDS DETERMINED BY DSC AND POLARIZED OPTICAL MICROSCOPY/, Thermochimica acta, 267, 1995, pp. 259-268
The crystallization process of poly(ethylene oxide) (PEG) and PEO/poly
(methyl methacrylate) (PMMA) blends in the low molecular weight region
of PEO was studied by differential scanning calorimetry (DSC) and pol
arized optical microscopy (POM). The half-time of the crystallization
t(1/2), the time at which crystallinity X(t) = 1/2, was inversely prop
ortional to the linear growth rate G of spherulite, i.e. t(1/2)(-1) pr
oportional to G. The value of E characterizes the temperature dependen
ce of the activation energy for the formation of a secondary nucleus o
n the growing side surface of the crystal lamella and was evaluated fr
om the t(1/2) measured by DSC. The value of E of PEO was not affected
by blending PMMA. However, the slightly increasing tendency of E was o
bserved for PEO and PEO/PMMA blends with increasing molecular weight o
f PEO, M(PEO) This tendency may correspond to the crossover of E from
low molecular weight material to polymer.