Plasticization and reinforcement in a boron cage compound polyurethane nanocomposite: A dielectric study

Abstract In order to control and modify the physical properties of nanocomposite systems, it is essential to understand the nano-filler/polymer structure–property relationships. Boron cage compounds (BCCs) are a class of icosahedral, closed cage molecules that are of interest due to their high boron content, their inherent neutron absorbing/shielding properties, their potential ability to act as molecular nano-particles and their ability to significantly improve the thermal stability of polymers in which they have been incorporated. When the BCC n -hexylcarborane is blended with a polybutadiene (PBD)/polyurethane (PU) segmented copolymer (EN8) an increase in the glass transition (T g ) temperature of the PBD phase (reinforcement) and a decrease in the T g temperatures of the PU phases (plasticization) are observed. These observations were investigated by examining the dielectric relaxation properties of copolymer samples with and without added n -hexylcarborane (0 wt.% and 5 wt.% n -hexylcarborane) using broadband dielectric spectroscopy in the frequency range from 0.01 Hz to 1 MHz and temperature range from − 140 to 130 °C. Parametric fitting techniques aided in the identification of two α relaxation processes associated with the glass transitions of the soft PBD phase and the hard urethane phases, and a secondary β relaxation process due to the localized motions of side groups. The conductivities at low frequencies were also identified and modeled. Differential Scanning Calorimetry (DSC) did not indicate the presence of a crystalline component within the copolymer samples, so interfacial polarization (Maxwell–Wagner–Sillars) relaxation is not possible. A relaxation map (Arrhenius diagram) associated with these processes has been developed from the experimental data to elucidate the role of n -hexylcarborane in the molecular dynamics of the system. Values of fitting parameters, calculated T g values, and a fragility index are also given for comparison. Reduced localized motion of the soft PBD phase, as well as reinforcement of the hard urethane phases is observed upon the introduction of n -hexylcarborane. The hypothesis that the n -hexylcarborane content preferentially locates within the hard urethane phases is supported by the observed decrease of the fragility index and T g of the urethane phases.