Ultrastabilization of a (rare-earth-loaded) faujasite (FAU)-type gallosilic
ate appears to be the only viable route for synthesizing a gallosilicate wi
th an acid site density comparable to that of ultrastable FAU-type aluminos
ilicates. Neither gallium insertion into a FAU-type silica nor substitution
of framework gallium by silicon using ammonium hexafluorosilicate appears
feasible. The ultrastable FAU-type gallosilicate shows no sites with enhanc
ed Bronsted acidity. According to the shift observed by IIE spectroscopy wh
en CO is adsorbed, the acid site strength of FAU-type gallosilicates is wea
ker than that of high-silica FAU-type aluminosilicates but stronger than th
at of FAU-type silicoaluminophosphates. Although the ultrastable FAU-type g
allosilicate is (hydro)thermally stable in an oxidizing atmosphere up to 11
50 K, it releases its gallium in a reducing atmosphere (starting at 525 K)
and loses structural integrity increasingly rapidly above 635 K. This sever
ely limits the potential use of catalysts based on gallosilicate framework
structures in hydrocarbon hydroconversion reactions.