The mechanism of FCC catalyst deactivation by sodium is addressed in this paper. In commercial units, sodium is found to deactivate the matrix surface area significantly but no significant trend was observed for the effect of sodium on the zeolite surface area of equilibrium catalysts. On the other hand, the effect of sodium is more pronounced on zeolite and much less severe on matrix surface area in the typical laboratory deactivation protocol. The differences are explained by the mobility of sodium on catalysts.Significant interparticle migration of sodium is observed both commercially and in laboratory deactivated catalysts. The loading of sodium is associated with the available sites of the particular fraction of that catalyst.In commercial units, sodium preferentially migrates to the freshly added catalyst due to its greater availability of exchange sites. The effect of catalyst sodium and feed sodium are simulated in the laboratory and their effect on catalyst activity and cracking yields are discussed.Sodium on fluid cracking catalyst, FCC, comes from the raw materials used in the catalyst manufacturing process as well as salt contamination in the feedstock. Sodium can deactivate cracking catalysts by poisoning the acid sites on the matrix and zeolite and by promoting sintering of silica-alumina (1). Sodium can act synergistically with vanadium to accelerate the destruction of zeolite (2).The relationship between cracking activity and sodium level of zeolites is complicated and seems to depend on the type of feedstock and catalyst