EVA was blended with phenoxy over the whole range of composition using a tw
in-screw Brabender. Two-phase separation caused by EVA crystallization was
observed in the EVA-rich blends and the dispersed domain of EVA was not cle
arly shown in the phenoxy-rich blends. Differential scanning calorimetry (D
SC) showed that the glass transition temperature (T-g) of EVA was increased
by 5-10 degrees C in the EVA-rich blends but the T-g of phenoxy was superp
osed over the melting behavior of EVA. X-ray diffraction measurement indica
ted that EVA crystallization was restricted in the phenoxy-rich blends and
the EVA crystal structure was influenced by incorporation of phenoxy into t
he EVA-rich blends. (C) 1999 John Wiley & Sons, Inc.