Effect of strontium contaminants upon the size and solubility of calcite crystals precipitated by the bacterial hydrolysis of urea.

The nucleation and growth of calcite precipitates induced by the bacterial hydrolysis of urea (ureolysis) from a Sr-contaminant inclusive, and a Sr-free artificial groundwater (AGW) mimicking the composition of the 90Sr contaminated Snake River Plain aquifer were investigated. Sr-free experiments exhibited a gradual increase in mean calcite crystal diameter (<1000 nm) from day (D) 1 to 6, while in the Sr-inclusive experiments, daily diameters were approximately constant from D1 to D6, and crystals were smaller (mean <840 nm). These data demonstrate a steady state had been attained early in the Sr-inclusive experiments from growth inhibition by Sr. Modeling of the crystal growth mechanisms on the USGS GALOPER software suggested crystal size distributions in the Sr-inclusive and Sr-free experiments were generated in the nucleation stage by a decreasing nucleation rate with surface-controlled growth, followed by supply-controlled and random growth. This occurred despite the availability of Ca2+ and HCO3-, implying crystal growth is limited bythe rate of solute advection to the crystal surface. Calculation of the solubility constant (In KsO(A)) demonstrates smaller crystals are more soluble, reflecting a higher molar surface area. The coprecipitation of Sr therefore generates smaller and thus more soluble crystals. However, this is unlikely to dramatically reduce the long-term effectiveness of Sr immobilization because when crystal growth had ceased in the Sr-inclusive AGW, > 99% of calcite precipitated and Sr coprecipitated occurred in large crystals with a low solubility.