Abstract
Nanosilica particles were dispersed into polymer diols by high pressure shearing homogenizer (HPSH), then polyurethane nanocomposites were prepared via in-situ polymerization of diphenylmethane diisocyanate (MDI) and polymer diols. FTIR analysis indicated that the -NCO groups of MDI had reacted with the hydroxy on the surface of nanosilica during in-situ polymerization. TGA suggested that polyurethane/nanosilica composites obtained by in-situ polymerization had better thermal stability than pure polyurethane. Meanwhile, the tensile and dynamic mechanical properties of the samples prepared by HPSH were superior to those by directly ultrasonic dispersing nanosilica, accompanied by more homogeneous dispersion of nanosilica particles in the polymer matrix.
ACKNOWLEDGMENTS
The work was financially supported by National Science and Technology Support Programs (No. 2007BAE22B02).