Ionic clathrate hydrates (ICHs) belong to one of the
groups of
a wide class of clathrate hydrates. In the crystal structures of ICHs,
cation–anion pairs of guest molecules, typically tetraalkylammonium/phosphonium
salts, are included into the host framework of hydrogen-bonded water
molecules. Because of their suitable phase change temperature and
latent heat, ICHs are considered as promising phase change materials
for application in cold energy storage and transportation. The presence
of vacant cavities in ICHs structures, which can incorporate small
gas molecules such as, for example, H2, CH4,
CO2, N2, H2S, determines the possibility
of their use for the separation and storage of gases. The formation
of these double ICHs occurs under much milder pressure and temperature
conditions compared to the pure gas hydrates of the same gases. Studying
of the structural characteristics and thermophysical properties of
ICHs and double ICHs with gases is the necessary basis for their effective
applications in different practical ends. This work reviews information
related to the new details and features of the structures of ICHs
and double ICHs with gases revealed over the last decade or a little
more as well as some thermophysical data such as hydrate numbers,
temperatures and enthalpies of dissociation. This review focuses only
on ICHs of tetrabutyl-, tetraisoamylammonium (TBA, TiAA), and tetrabutylphosphonium
(TBP) salts, which are the most common representatives of this class
of compounds. One of the sections is devoted to ICHs of TBA and TiAA
with polymeric anions such as cross-linked polyacrylates. The purpose
of the present paper is to review the studies that have been relatively
little addressed in previous works.