Two
biobased poly(hexamethylene 2,5-furandicarboxylate) (PHF)/multiwalled
carbon nanotube (MWCNT) composites, i.e., PHF/MWCNTs-0.25 and PHF/MWCNTs-0.5,
with the number indicating the weight ratio of nanofiller, were synthesized
through an in situ melt polycondensation method. MWCNTs were well
dispersed in the PHF matrix. The addition of low content of MWCNTs
significantly enhanced the nonisothermal and isothermal melt crystallization
behavior of PHF due to the filler as a nucleation agent, which led
to higher melt crystallization temperatures at an indicated cooling
rate and faster crystallization rates at the same isothermal crystallization
temperature. The crystallization half-time significantly decreased
from about 35 min for PHF to 1.5 min for PHF/MWCNTs-0.5 at 130 °C.
However, the crystal structure and crystallization mechanism of PHF
remained unchanged. In addition, MWCNTs remarkably affected the tensile
and dynamic mechanical properties of PHF.