It is found that polypropylene yields can be increased by a factor of
two to three by introducing KCl into the catalytic system l4/MgCl2/eth
ylbenzoate-AlR3/p-methoxyethylbenzoate (R = iso-Bu, Et) during propyle
ne polymerization. In this case, the fractional composition of polypro
pylene, its molecular weight, and characteristics of stereoregularity
of the isotatic fraction are not changed. The activation effect of KCl
is explained by its ability to form complexes with AlR2Cl, which are
produced in the system via catalyst alkylation. AlR2Cl is not a cocata
lyst. The time dependence of the rate of propylene polymerization is s
atisfactorily described by a second-order formal kinetic equation. The
activation of the system is presumed to be assoicated with the stabil
ization of active sites, i.e., with a decrease in the deactivation rat
e constant, rather than with an increase in the propagation rate const
ant and in the number of active sites.