Studies on the synthesis of ZSM-5 by interzeolite transformation from zeolite Y without using organic structure directing agents

In this work, a study of the interzeolite transformation from a parent zeolite Y (FAU topology) into zeolite ZSM-5 (MFI topology) was carried out, without using organic structure directing agents, by addition of SiO2 to adjust the composition of the starting gel. Depending on the SiO2/Al(2)O3( )molar ratio, zeolite Y can be present in amounts equivalent to those of seed-assisted syntheses. Zeolite Y was successfully transformed in ZSM-5, but a rigorous control of OH-/SiO2 and Na+/SiO2 molar ratios is necessary to avoid incomplete transformation and/or contamination by layered silicates, such as magadiite and kenyaite. For hydrothermal treatment duration lesser than 12 h, the phase dissolution of the Y zeolite is observed, resulting in amorphous phase after 24 h. From 48 h, nucleation and growth of ZSM-5 crystals, with increasing crystallinity up to 120 h, is observed. During the interzeolite transformation, FTIR spectra show the disappearance of the band at 568 cm(-1) and the appearance of a band at 545 cm(-1), assigned to the 5-membered double rings of ZSM-5. Scanning electron microscopy images suggest that the crystallites of zeolite Y condense and absorb silicate species from solution to form larger aggregates of ZSM-5 zeolite. These structural and morphological changes are accompanied by textural changes detected in nitrogen adsorption isotherms. These results suggested that a combined solution mediated and solid-state transformation mechanism is probably occurring. Since these zeolites do not possess any other structural features in common, RBU approach seems to be more adequate to describe this specific interzeolite transformation.