Catalytic cracking of hydrocarbons takes place via elementary reaction
s such as initiation processes to form carbenium ions, olefin adsorpti
on/desorption steps, isomerization, beta-scission, oligomerization, an
d hydride ion transfer steps. These elementary steps involving reactiv
e carbenium ion surface intermediates are the essential components of
catalytic cracking that lead to various catalytic cycles and their cor
responding stoichiometric reactions. This review outlines methods used
to quantify reaction kinetics for catalytic cracking and describes ho
w the rates of specific catalytic cycles are controlled by catalyst tr
eatment (e.g., steaming) and process conditions (e.g., conversion and
temperature).