We studied the nucleation of polypropylene via experimental measuremen
ts and molecular modeling, and we propose that sugar acetal nucleators
stabilize the helical form of polypropylene at the molecular level. T
hrough FTIR techniques, we established that the nucleators dibenzylide
ne sorbitol (DBS) and trinaphthylidene sorbitol are chemically stable
in molten polypropylene. Using solid-state NMR, we determined that DBS
is dispersed to particles 32 angstrom in diameter. These particles ar
e three orders of magnitude smaller than the 1-10-mum size expected in
the literature. DSC was employed to evaluate the nucleating ability o
f our nucleators. Through molecular modeling, we demonstrated that nuc
leating ability can be correlated with van der Waals attractions of th
e individual nucleator molecules with the helical form of polypropylen
e. A correlation was not seen when hydrogen bonded nucleator dimers we
re used. The model correctly predicted that one TNS diastereomer nucle
ates polypropylene and that the other diastereomer does not.