Abstract

This document provides information specific to H-Area waste tanks that enables a flow and transport model with limited chemical capabilities to account for varying waste release from the tanks through time. The basis for varying waste release is solubilities of radionuclides that change as pore fluids passing through the waste change in composition. Pore fluid compositions in various stages were generated by simulations of tank grout degradation. The first part of the document describes simulations of the degradation of the reducing grout in post-closure tanks. These simulations assume flow is predominantly through a water saturated porous medium. The infiltrating fluid that reacts with the grout is assumed to be fluid that has passed through the closure cap and into the tank. The results are three stages of degradation referred to as Reduced Region II, Oxidized Region II, and Oxidized Region III. A reaction path model was used so that the transitions between each stage are noted by numbers of pore volumes of infiltrating fluid reacted. The number of pore volumes to each transition can then be converted to time within a flow and transport model. The bottoms of some tanks in H-Area are below the water table requiring a differentmore » conceptual model for grout degradation. For these simulations the reacting fluid was assumed to be 10% infiltrate through the closure cap and 90% groundwater. These simulations produce an additional four pore fluid compositions referred to as Conditions A through D and were intended to simulate varying degrees of groundwater influence. The most probable degradation path for the submerged tanks is Condition C to Condition D to Oxidized Region III and eventually to Condition A. Solubilities for Condition A are estimated in the text for use in sensitivity analyses if needed. However, the grout degradation simulations did not include sufficient pore volumes of infiltrating fluid for the grout to evolve to Condition A. Solubility controls for use in a flow and transport model were estimated for 27 elements in each of the chemical stages generated in the grout simulations plus local groundwater. The grout simulations were run with the initial infiltrating fluid in equilibrium with atmospheric oxygen to account for degradation of the reduction capacity of the grout. However, a lower Eh was used in pore fluids in the oxidizing conditions used to estimate solubilities to be more consistent with measured Eh values and natural systems. Solubilities of plutonium are affected by this decision, but those of other elements are not. In addition, the baseline for H-Area tanks is that they will be washed with oxalic acid prior to being filled with grout. Hence, oxalate was included in the pore fluids by assuming equilibrium with calcium oxalate. Solubility estimates were done by equilibrating a solubility controlling phase for each element with the pore fluid compositions using The Geochemist’s Workbench®. Condition B pore fluids are similar to Condition D. Therefore, solubilities for Condition B were not estimated, but assumed to be the same as in Condition D. In general solubility controlling phases were selected to bias solubilities to higher values. Several elements had no solubility controls and solubility estimates for other elements were omitted because the elements had short half-lives or were present in residual waste in very low amounts. For these it is recommended that release from the tank be instantaneous when the tank liner is breached. There is considerable uncertainty in this approach to enabling a flow and transport model to account for variable waste release. Yet, it is also flexible and requires much less computing time than a fully coupled reactive transport model. This allows some of the uncertainty to be addressed by multiple flow and transport sensitivity cases. Some of the uncertainties are addressed within this document. These include uncertainty in infiltrate composition, grout mineralogy, and disposition of certain components during the simulations. Uncertainty in the solubility estimates is addressed in part by examining sensitivity of solubilities for four key elements to uncertainty in thermodynamic data, pH, Eh, total inorganic carbon concentration, and oxalate concentration. In addition, the solubilities for the elements estimated here are compared to two other compilations of solubilities in cementitious materials.« less

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