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Salt Disposal of Heat-Generating Nuclear Waste

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epositories using thermodynamic models. For example, some <strong>of</strong> the constituents<br />

listed in Table 3 differ from what is included in the current geochemical models<br />

for salt repositories. When additional, major constituents (i.e., those that expand<br />

the chemical system) are introduced, the emphasis <strong>of</strong> geochemistry research<br />

would be the consistent compilation/derivation <strong>of</strong> the relevant thermodynamic<br />

data and other parametric values needed for representing concentrated brine<br />

systems (e.g., Pitzer parameters).<br />

One <strong>of</strong> the overriding advantages <strong>of</strong> salt disposal is the absence <strong>of</strong> brine.<br />

However, it may be possible to develop a scenario by which the repository<br />

resaturates after the thermal period. The volume <strong>of</strong> brine depends on the<br />

mechanism bringing brine into the repository and whether or not the repository<br />

has removed nearly all the void space by plastic deformation and reconsolidation.<br />

For a disturbed scenario where an aquifer in the vicinity <strong>of</strong> the repository may be<br />

breached in some way, open and connected repository space could fill with brine.<br />

Important chemical conditions occur only if ample brine is available to the<br />

system.<br />

Chemical conditions in a repository can be described based on the predicted<br />

chemical reactions among the solids, liquids, and gases present in the system. For<br />

a salt repository, this translates into characterizing the reactions among the solid<br />

phases found in the salt formation, the solid phases that are the waste, the waste<br />

package and the emplacement materials, the brines that are in equilibrium with<br />

the salt formation solid phases, and the gases that may be present as part <strong>of</strong> the<br />

formation or may be introduced into the repository during construction.<br />

The host rock <strong>of</strong> a bedded salt repository is, typically, dominantly composed <strong>of</strong><br />

halite (NaCl) with significant amounts <strong>of</strong> anhydrite (CaSO 4 ), polyhalite<br />

(K 2 MgCa 2 (SO 4 ) 4 •2H 2 O), and clay minerals as minor phases. The thermodynamic<br />

properties <strong>of</strong> halite and anhydrite are well known. To the extent that polyhalite<br />

and clay minerals are present in the formation, their thermodynamic properties<br />

would be part <strong>of</strong> a geochemical model, and their associated uncertainties would<br />

contribute in a fractional manner to the overall uncertainty in the results.<br />

<strong>Salt</strong> formation brines tend to have high concentrations <strong>of</strong> sodium, calcium, and<br />

chloride. Lesser amounts <strong>of</strong> sulfate and carbonate are present. Some brines also<br />

have high magnesium concentrations. Recently, ongoing research has shown that<br />

borate is an important component in WIPP brines.<br />

The in situ pH <strong>of</strong> brines is slightly acidic (i.e., about 6.0 to 6.5). Mineral<br />

components <strong>of</strong> the salt formation buffer the pH to their in situ values. The pH <strong>of</strong><br />

brines after interaction with steel waste packages at low temperatures would<br />

probably be similar to that characteristic <strong>of</strong> the brucite “half buffer” used at WIPP<br />

(pH <strong>of</strong> about 9). The pH <strong>of</strong> brines in contact with steel waste packages at high<br />

temperatures may need to be determined. <strong>Heat</strong>ing the brine would change the pH.<br />

If buffered by mineral or gas equilibria, the pH would shift with temperature<br />

according to the applicable equilibrium constants in a predictable manner. Buffer<br />

45

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