Blends of linear low-density polyethylene (LLDPE) and very low-density poly
ethylene (VLDPE) with long chain branching have been prepared by extrusion
mixing. All copolymers have similar branch lengths and are commercial ethyl
ene-octene copolymers. The copolymers and blends were subjected to crystall
isation ("thermal fractionation") by stepwise cooling interspersed with iso
thermal periods and the fractionated samples were examined by differential
scanning calorimetry (DSC). Thermal fractionation by DSC separates copolyme
rs and blends according to their branching densities. Thermal fractionation
data were used to calculate branching distribution in polyethylenes using
calibration curves obtained from the literature. It is found that LLDPE con
tains a broad distribution of branching densities whereas the VLDPEs contai
n a narrow distribution, though with shorter average lengths between branch
es. Where both polymers have common melting endotherms in the thermally fra
ctionated blends they may co-crystallise if they are mutually miscible in t
he melt. In blends containing low amounts of VLDPEs, the branching observed
are combined effects of each individual polymer indicating that polymers r
etain some of their individual features after blending. The blends with hig
h VLDPE amounts show some miscibility in the melt suggesting co-crystallisa
tion between the copolymers may be occurring. (C) 2000 Elsevier Science Ltd
. AU rights reserved.