Boiling of natural zeolites at high temperatures is the major peculiarity b
y which they are recognized and From which they derived their name. The mic
romechanism of this process was studied by IR spectroscopy. It has been est
ablished that the source of the gas phase in the process is not the initial
"zeolite water", as supposed earlier, but the product of its high-temperat
ure evolution, which passes through three stages: 1) dissociation of the "z
eolite water" (released during partial dehydration of the zeolite) under th
e action of the electrostatic field of the coordinatively unsaturated polyv
alent cations; 2) hydroxylation of the aluminosilicate framework; 3) dehydr
oxylation of the latter with release of gas H2O. This gas phase causes boil
ing of natural zeolites at high temperatures as they reach a pyroplastic st
are. Small polyvalent cations, such as Ca2+, Mg2+ etc., play an important r
ole in high-temperature hydroxylation of zeolites and, correspondingly, in
their boiling, as they have a high charge density and, hence, a high polari
zation capacity.