MOLECULAR-ORIENTATION IN DEFORMED BIMODAL NETWORKS .2. FOURIER-TRANSFORM INFRARED MEASUREMENTS ON POLY(DIMETHYLSILOXANE) NETWORKS AND COMPARISON WITH THEORY

Citation
S. Besbes et al., MOLECULAR-ORIENTATION IN DEFORMED BIMODAL NETWORKS .2. FOURIER-TRANSFORM INFRARED MEASUREMENTS ON POLY(DIMETHYLSILOXANE) NETWORKS AND COMPARISON WITH THEORY, Macromolecules, 28(1), 1995, pp. 231-235
Citations number
15
Categorie Soggetti
Polymer Sciences
Journal title
ISSN journal
00249297
Volume
28
Issue
1
Year of publication
1995
Pages
231 - 235
Database
ISI
SICI code
0024-9297(1995)28:1<231:MIDBN.>2.0.ZU;2-Q
Abstract
Results of segmental orientation in uniaxially stretched bimodal poly( dimethylsiloxane) networks are reported. Measurements are carried out by Fourier transform infrared dichroism spectroscopy. Bimodal networks were formed by tetrafunctionally end-linking low molecular weight (M( n) = 5600) deuterated chains with high molecular weight (M(n) = 20000) hydrogenated chains. Independent measurements of segmental orientatio n of the short and the long chains showed that the short (long) ones o rient less (more) than the corresponding chains of the unimodal networ ks, in conformity with the predictions of the theory developed in the preceding paper. Furthermore, the change in segmental orientation of s hort and/or long chains in bimodal networks relative to their unimodal counterparts, expressed by the ratios S-S/S-S degrees or S-L/S-L degr ees is in reasonable quantitative agreement with the theory. Experimen ts show that the orientations of the short and the long chains in bimo dal networks are approximately equal to each other. On the other hand, the theory based on the phantom network model theory and experiments i s observed in the case of longer chains, whose behavior does ndt confo rm with the phantom network model underlying the theory. The differenc es between theory and experiments are attributed to the effects of ent anglements which operate to different extents for different chain leng ths.