The effect of the surface charge of nucleation agents on the crystallization behavior of poly(vinylidene fluoride) (PVDF) has been investigated. Ion-dipole interaction between the positive surface of nucleation agents and the partially negative CF(2) dipoles of PVDF is established as a main factor for further lowering the free energy barrier for nucleation, and thus increasing significantly the crystallization kinetics. This is in contrast to the behavior observed for nucleation agents possessing either negative surface or neutral charges.
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