The heat shrinkability of polymers is utilised in Various applications-main
ly in the field of encapsulation. Elastic memory is introduced into the sys
tem by means of an elastomeric phase. Here, blends of ethylene vinyl acetat
e (EVA) and epichlorohydrin were studied with reference to their shrinkabil
ity, by introducing crosslinking in the elastomer phase. It was found that
an increase in elastomer content and cure time caused the shrinkage to incr
ease. High temperature (H-T) stretched samples showed higher shrinkage than
room temperature (R-T) stretched ones. Generally the crystallinity of high
temperature (H-T) stretched samples was higher than that of low temperatur
e stretched ones which was again higher than that of the original unstretch
ed samples. From high temperature DSC it was found that with increase in ep
ichlorohydrin content, stability towards oxygen was decreased and for high
temperature stretched samples, the stability was increased compared to the
original unstretched and high temperature shrunk samples. But for H-T shrun
k samples the first and second decomposition temperatures were lower and th
e rate of degradation was enhanced compared to unstretched samples and H-T
stretched ones. SEM showed that H-T stretched samples were more elongated t
han R-T stretched ones.