Ma. Sherman et Jp. Kennedy, NOVEL PALYISOBUTYLENE POLY(DIMETHYLSILOXANE) BICOMPONENT NETWORKS - II - NETWORK STRUCTURE AND PROPERTY CHARACTERIZATION/, Journal of polymer science. Part A, Polymer chemistry, 36(11), 1998, pp. 1901-1910
The first part of this series concerned the synthesis of novel polyiso
butylene (PIB)/poly(dimethylsiloxane)( PDMS) bicomponent networks; the
present paper concerns the structure and property characterization of
a series of bicomponent networks of varying compositions (PIB wt %/PD
MS wt % = 92/8, 70/30, 50/50, 35/65) having average molecular weights
between crosslinks ((M) over bar(c)) of similar to 20,000 g/mol. Accor
ding to network structure analysis by uniaxial equilibrium stress-stra
in measurements, the experimental (M) over bar(c)'s are in excellent a
greement with theoretical values. Hydrosilation end-linking efficiency
was quantitated by the amount of sol and functional group analysis by
H-1-NMR spectroscopy. NMR evidence indicates double-bond isomerizatio
n during hydrosilation. Network compositions by elemental analysis tog
ether with the low sol fractions indicate efficient crosslinking. Thes
e data suggest highly efficient network formation and well-defined bic
omponent network structures. While PIE and PDMS showed T-g's at -72 an
d -124 degrees C, respectively, the bicomponent network did not exhibi
t clearly discernible phase transitions. The heat stability of bicompo
nent networks increased slightly with increasing PDMS content showing
initial (10%) degradation temperatures at similar to 380 degrees C in
nitrogen and similar to 320 degrees C in air. Tensile strengths and el
ongations were dependent on composition and varied in the 0.6-3.8 MPa
and 600-1100% ranges, respectively. The swelling behavior was not much
affected by composition. (C) 1998 John Wiley & Sons, Inc.