Author/Authors :
Luciana Tavares dos Santos، نويسنده , , Fabiana M. Santos، نويسنده , , Raphael S. Silva، نويسنده , , Thiana S. Gomes، نويسنده , , Pierre M. Esteves، نويسنده , , Ricardo D.M. Pimenta، نويسنده , , Sonia M.C. Menezes، نويسنده , , Oscar R. Chamberlain، نويسنده , , Yiu L. Lam، نويسنده , , Marcelo Maciel Pereira، نويسنده ,
Abstract :
The regeneration of a coked fluid catalytic cracking (FCC) catalyst under O2/He and CO2/He atmospheres from room temperature up to 1000 °C was studied using online mass spectroscopy. The catalyst was also thermally treated at temperatures between 300 °C and 500 °C in order to promote coke modification. It was verified that the amount of aliphatic carbon decreased for higher temperatures. These treatments have a more significant impact on the coke-CO2 reaction than on the coke-O2 reaction. The former reaction was the focus of the present investigation and the results were compared to the latter reaction. CO2 preferentially reacts in the beginning of coke burning and a remarkable decrease of CO2 activity is observed with the calcinated coked catalyst. Regeneration under 13CO2/He at constant temperatures between 600 °C and 940 °C revealed a first-order kinetics for the coke-CO2 reaction. The CO2 molecule reacts dissociatively introducing oxygenated functionality into the coke. These species are decomposed at high temperature forming CO and no water is observed during the CO2-coke reaction.