Efficient Dry Impregnation of Zirconium into H‐ZSM‐5 Zeolites

Abstract

There is considerable interest in adjusting the acidity and pore architecture of zeolites. Herein, we present solventless incorporation of zirconium (∼2–10 wt.%) in a precursor and desilicated (0.2 and 0.4 mol L−1 NaOH) H‐ZSM‐5 zeolite. Infrared and UV‐vis‐DR spectroscopy confirmed the grafting of highly dispersed Zr in all the zeolites. XRD indicated the presence of ZrO2 in zeolites with higher Zr contents. The micropore volume of the precursor zeolite decreased by ∼10 %, suggesting the presence of Zr mainly on the external surface, while it decreased more than 20 % for the desilicated sample, suggesting Zr had access to the micropores at higher Zr contents. Infrared spectroscopy after pyridine adsorption provided evidence for the Brønsted and Lewis acid sites in all zeolites, but the Brønsted acid‐to‐Lewis acid site ratio decreased by >50 % depending on the Zr and NaOH concentrations. The presence of Zr critically changed the predominant nature of the acid sites of the desilicated zeolites.