ABSTRACT:The phase behavior and rheological behavior of low molar mass liquid crystal (LLC) and polycarbonate blends is firstly reported. The results of small angle light scattering (SALS) indicate that the LLC is miscible in the mixture for weight fractions of LLC less than 6%. Mixtures of two different liquid crystals with two different molecular weight of polycarbonate were prepared inside the miscible regime of the blends. Both the complex and steady shear viscosities of the blends were found to be significantly decreased upon addition of small amounts of liquid crystal (1% by weight). At low shear rate, the steady state shear viscosity was similar to the pure polycarbonate, whilst, at higher shear rates, three further regimes of behavior, as has been described for liquid crystals and liquid crystal polymers, were found despite the low concentration of LLC; hence, the rheological properties of the blends can be significantly modified by small concentrations of LLC (as low as 1%). The decrease in melt viscosity of polycarbonate that we observe upon addition of LLC is not due to lubrication effects at the interfaces, as shown by reproducible oscillatory shear flow sweeps.

The melt rheology of blends of a low molar mass liquid crystal (LC) blended with bisphenol A-polycarbonate (PC), and the self-diffusion of the polycarbonate in the blends are reported. Results of small angle light scattering indicate that the LC is miscible in the mixture for weight fraction of LC less than 6%. The rheological properties of the blended sample within the miscible regime of the blends vary significantly with LC content. Although at low shear rates, the viscosity is similar to that of the pure polycarbonate, at high shear rates the curves show three regions of behavior, as has been described previously for pure LCs. The diffusion coefficient was obtained from interdiffusion studies using nuclear reaction analysis of bilayer films. An addition of only 1 wt % LC to the polycarbonate significantly increased the diffusion coefficient, but at higher concentration the converse was found.

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