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