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DOE-HDBK-1129-99
flow rate and lifetime requirements. The basic strategy currently being implemented in prototype
systems is to crack the molecules on a hot getter and remove the non-tritiated reactive impurities
that interfere with the performance of the hydrogen gettering alloys. Following purification, the gas
is passed through a hydrogen gettering bed to remove the hydrogen isotopes from the gas stream.
2.5.2.b(6) LaNi5 Based Alloys
The use of lanthanum-nickel hydrides has been a continuing topic of interest, and as recently as
1997, promising results for hydrogen storage have been reported ("LaNi5 Intermetallic Hydride,"
extracted from State-of-the-Art Review of Hydrogen Storage in Reversible Metal Hydrides for
Military Fuel Cell Applications, Gary Sandrock, Ph.D., for the Department of the Navy, Office of
Naval Research, N00014-97-M-0001, July 24, 1997). Promising research results were also
reported in the literature in 1988 ("Hydrogen Isotope Sorption Properties of LaNi3Mn2 Alloy as a
Candidate for the Tritium Storage Material," T. Ide et al., Sumitomo Heavy Industries, Ltd. and H.
Yoshida et al., Japan Atomic Research Institute, published in Fusion Technology, September
1988). Earlier research at Mound, however, in the 1970s and early 1980s indicated that
lanthanum-nickel-based alloys were not appropriate for tritium service due, in part, to
disproportionation. When cycled, the LaNi5 had a tendency to separate to form the parent metals
(La or Ni) or different alloys. The disproportionation tended to change the pressure, concentration,
and temperature properties of the metal/alloy mix and increase the quantity of tritium bound in the
heel that was not easily recoverable.
Further investigations will be needed to better ascertain the capabilities of LaNi alloys for tritium
service.
2.5.2.c Absorbed Water
Molecular sieve material is used in tritium removal systems for removal of water contaminated with
tritium. Systems such as tritium removal systems, effluent recovery systems, and cleanup systems
remove tritium from a gas by cracking the tritium-containing components on a heated precious
metal catalyst. The free tritium then combines with oxygen in the gas stream to form tritiated
water. The gas stream is then cooled to room temperature, and the water contained in the gas
stream, including the tritiated water, is removed by a molecular sieve trap.
A molecular sieve will hold about 18 percent water by weight, and the sieve may be regenerated to
remove the water so it can be reused. The issue of flammability limits of these containers is
discussed in Section 3.1.2. Tritiated water absorbed on molecular sieve is not corrosive and may
be stored in this way for long periods without damage to the container wall.
Water contaminated with HTO is also stored on clay. The common method of solidification of
tritium-contaminated wastewater for disposal is to solidify the water on clay so that it can be
classified as solid waste. Clay will hold approximately 60 percent water by volume. Waste
disposal sites generally require the use of 100 percent more clay than required to solidify the
water, and, as a result, the water is generally limited to 30 percent of the volume of the clay for
waste solidification purposes. Water absorbed on clay is not corrosive and may be stored for long
periods without damage to the container wall.
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