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Evaporative Concentration of 100x J13 Ground Water at 60% Relative Humidity and 90C.

by S. A. Carroll, M. Sutton, Q. A. Nguyen, P. Hailey, K. Staggs, Maureen Alai ยท 2003

ISBN:  Unavailable

Category: Unavailable

Page count: 15

In these experiments we studied the behavior of a synthetic concentrated J13 solution as it comes in contact with a Ni-Cr-Mo-alloy selected for waste canisters in the designated high-level nuclear-waste repository at Yucca Mountain, Nevada. Concentrated synthetic J13 solution was allowed to drip slowly onto heated test specimens (90 C, 60% relative humidity) where the water moved down the surface of the specimens, evaporated and minerals precipitated. Mineral separation or zoning along the evaporation path was not observed. We infer from solid analyses and geochemical modeling, that the most corrosive components (Ca, Mg, and F) are limited by mineral precipitation. Minerals identified by x-ray diffraction include thermonatrite, natrite, and trona, all sodium carbonate minerals, as well as kogarkoite (Na{sub 3}SO{sub 4}F), halite (NaCl), and niter (KNO{sub 3}). Calcite and a magnesium silicate precipitation are based on chemical analyses of the solids and geochemical modeling. The most significant finding of this study is that sulfate and fluoride concentrations are controlled by the solubility of kogarkoite. Kogarkoite thermodynamic data are needed in the Yucca Mountain Project database to predict the corrosiveness of carbonate brines and to establish the extent to which fluoride is removed from the brines as a solid.