Catalytic deactivation in gas phase propylene polymerization with CSBR
was investigated in two concepts of chemical and physical ways. In ki
netic consideration, catalyst deactivation followed the 2nd order reac
tion due to chemical phenomenon like active site reduction. In case of
physical consideration, catalyst deactivation was progressed by monom
er diffusion resistance. It was due to formation of dense IPP around c
atalyst at the beginning of polymerization. There were excessive monom
er concentration differences between catalyst and polymer surfaces unt
il 90 min after initial polymerization. Consequently, the main reason
of catalyst deactivation is not only chemical phenomenon, but also phy
sical one such as monomer diffusion resistance.