ISOTACTIC POLYPROPYLENE HYDROGENATED OLIGO (CYCLOPENTADIENE) BLENDS .1. THERMAL AND DYNAMIC-MECHANICAL BEHAVIOR OF ANNEALED SAMPLES

Citation
A. Cecere et al., ISOTACTIC POLYPROPYLENE HYDROGENATED OLIGO (CYCLOPENTADIENE) BLENDS .1. THERMAL AND DYNAMIC-MECHANICAL BEHAVIOR OF ANNEALED SAMPLES, Polymer, 33(7), 1992, pp. 1411-1417
Citations number
15
Journal title
ISSN journal
00323861
Volume
33
Issue
7
Year of publication
1992
Pages
1411 - 1417
Database
ISI
SICI code
0032-3861(1992)33:7<1411:IPHO(B>2.0.ZU;2-D
Abstract
Blends of isotactic polypropylene and hydrogenated oligo(cyclopentadie ne) were prepared by melting-mixing in a Brabender-like apparatus. She ets of such blends were moulded under pressure, quenched in water and then annealed for 24 h at 140-degrees-C. Wide angle X-ray scattering w as used to examine the effect of the annealing treatment on the quench ed specimens. Thermal properties were analysed using a differential sc anning calorimeter. Melting points and overall crystallinity content d ecreased linearly up to a content of 50% in water of HOCP. Beyond such a value a further decrease was observed. Dynamic-mechanical tests wer e performed at various frequencies (in the range 1 x 10(-2)-75 Hz) and at different temperatures (from -40-degrees-C to 120-degrees-C). The two components appeared to be compatible in the amorphous regions of t he system, as already suggested in the literature. In fact a unique pe ak of the loss modulus versus temperature (which is representative of the glass transition temperature), was always present. Moreover the ma ximum of the peak was shifted to higher temperatures with increasing o ligomer content. The most interesting feature, however, was the change in shape of the whole curve. In fact the peak broadened more and more whereas the height increased only slightly as the oligomer percentage was increased. A tentative explanation is given in the present paper in terms of particular features of the blend morphology, and of a phas e inversion at high HOCP content in the blends.