Various radionuclides
are released as gases during reprocessing
of used nuclear fuel or during nuclear accidents including iodine-129
(
129
I) and iodine-131 (
131
I). These isotopes
are of particular concern to the environment and human health as they
are environmentally mobile and can cause thyroid cancer. In this work,
silver-loaded heat-treated aluminosilicate xerogels (Ag-HTX) were
evaluated as sorbents for iodine [I
2(g)
] capture. After
synthesis of the base NaAlSiO
4
xerogel, a heat-treatment
step was performed to help increase the mechanical integrity of the
NaAlSiO
4
gels (Na-HTX) prior to Ag-exchanging to create
Ag-HTX xerogels. Samples were characterized by powder X-ray diffraction,
scanning electron microscopy, energy-dispersive X-ray spectroscopy,
transmission electron microscopy, Brunauer–Emmett–Teller
analysis, gravimetric iodine loading, nanoindentation, and dynamic
mechanical analysis. The structural and chemical analyses of Ag-HTX
showed uniform distribution of Ag throughout the gel network after
Ag-exchange. After I
2(g)
capture, the AgI crystallites
were observed in the sorbent, verifying chemisorption as the primary
iodine capture mechanism. Iodine loading of this xerogel was 0.43
g g
–1
at 150 °C over 1 day and 0.52 g g
–1
at 22 °C over 33 days. The specific surface
area of Ag-HTX was 202 m
2
g
–1
and decreased
to 87 m
2
g
–1
after iodine loading. The
hardness of the Na-HTX was >145 times higher than that of the heat-treated
aerogel of the same starting composition. The heat-treatment process
increased Young’s modulus (compressive) value to 40.8 MPa from
7.0 MPa of as-made xerogel, demonstrating the need for this added
step in the sample preparation process. These results show that Ag-HTX
is a promising sorbent for I
2(g)
capture with good iodine
loading capacity and mechanical stability.