At room temperature, gaseous Fi extracts tetrahedrally coordinated aluminum
from the lattice of an acid, near-faujasite HY zeolite (Si/Al approximate
to 13) and forms fluoro-hydroxy-aluminum complexes of the type Al2F(OH)(n)(
(5-n)+) in which Al is octahedrally coordinated. Moreover, the crystallinit
y of the zeolite is almost unchanged by the fluorination process. The HY de
hydrated at 200 degreesC under vacuum and treated under a F-2 pressure of 3
00 mbar at room temperature is practically totally dealuminated. At lower p
ressure the transformation is partial. The coordination shell of the comple
x becomes unstable at about 500 degreesC. Upon losing ligands, octahedral A
l reverts partially to the tetrahedral coordination and is partially reinse
rted into the lattice. At a higher temperature an amorphous alumina phase i
s formed. Al-27 and F-19 high-resolution solid-state NMR, FT-IR, X-ray diff
raction, and temperature-programmed desorption (TPD) are the main tools use
d in this work. (C) 2001 Academic Press.