Abstract

In this work, the hydrogen transfer activity of two series of HY zeolites dealuminated by steam and by SiCl 4 (24.47-24.24 Å unit cell) has been measured from the butene/butane ratio in the products obtained during the cracking of a vacuum gas oil at 756 K. With the steam-dealuminated zeolites, a sharp decrease in the ratio of hydrogen transfer to cracking is observed when the number of Al atoms per unit cell falls below 10. On the other hand, in samples dealuminated by SiCl 4, this ratio changes very little with dealumination. These results cannot be explained assuming the need for adjacent acid sites for the hydrogen transfer. We have found, by adsorption measurements of n-butane and 1-butene, that the changes in the relative rates of bimolecular (hydrogen transfer) to monomolecular (cracking) reactions, observed with dealuminated HY zeolites, can be explained by the changes in the adsorption capacity and adsorption selectivity which occur on zeolites dealuminated at different levels by different dealumination procedures, and which are due to changes in the electric fields inside the pores.

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