NMR and IR Studies of Zeolite H-ZSM-5 Modified with Orthophosphoric Acid

By combined use of solid-state NMR, NMR self-diffusion techniques, and diffuse reflectance IR spectroscopy, important information on the nature of the interaction of orthophosphoric a id with zeolite H-ZSM-5 could be obtained. By aH NMR self-diffusion experiments it was found that the phosphoric acid enters the ZSM-5 channel system. However, with increasing amounts of H3PO 4 deposited, there is an enrichment of phosphorus pecies near the external surface of the zeolite crystals, forming a transport barrier for diffusing molecules. 27A1 MAS NMR shows that the decreased concentration f BrCnsted acid sites in H-ZSM-5 after impregnation with orthophosphoric acid and a subsequent thermal treatment at 500°C is a direct result of a framework dealumination. Combined 27A1, 29Si, 3ip, and 1H MAS NMR studies reveal that this dealumination process is promoted by the presence of increasing amounts of H3PO4 and results in the formation of occluded aluminum phosphate species. Furthermore, IH MAS NMR shows that H3PO 4 impregnation causes a drastic reduction in the concentration f nonacidic silanol groups. Both findings of 1H MAS NMR have been verified by diffuse reflectance IR spectroscopy. Consequently, treatment of ZSM-5 with orthophosphoric a id modifies acidity and diffusivity in the sample series under study. These effects can combine to give a useful catalyst of enhanced paraselectivity. © 1990 Academic Press, Inc