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' BMRI--San Luis <br />1998 Backfip Geochemi.~ry <br />' rate for sulfate from the gneiss in the backfill would be 274.5 mg SO< per kg of rock, <br />or 0.275 g SO. per kg of pink gneiss. <br />The total mass of backfill in the West Pit is 5,779,207 tons (R. Zumwalt, personal <br />communication, 29 Oct 1998). One US ton is 0.91 E+3 kg. Therefore the total mass <br />' of solid backfill is 5.26 E+9 kg rock. To be very conservative, it is assumed that all <br />of this rock could produce as much sulfate to solution as the median value for the pink <br />gneiss. Therefore, the total mass of sulfate that could be released from the backfill <br />' would be 1.45 E+9 g SO.. In fact, not all of the backfill is gneiss, and so tit e <br />calculated total mass o_f sulfate released for the backfill_- assuming all of the material <br />is i ~ - is co e. It also is likely t~Ftai the backfilled rock had not fully <br />' reacted before being inunda , as the more rigorously oxidized HCT samples surely <br />did, so the conservatism of this analysis more than offsets the use of the medilan value <br />' rather than the maximum value. <br />Assuming that the density of intact rock is about 2.6 g/cm' (2.6 E+3 kg/m3), the <br />' volume of intact rock equivalent to the backfill would be 2.02 E+6 m'. BMRI <br />estimate a swell factor for the backfill of 33% (R. Zttrnwalt, personal communication, <br />29 Oct 1998), so the total volume occupied by the backfill is approximately 2.69 E+6 <br />' m'. Therefore, the effective porosity of the backfilled mass is 0.33, and the notal <br />volume of water in the backfill is 8.88 E+5 m'. ~,,,,.n. ,o::.nn,~ ~ ¢~-r~H <br />Concentration is the mass of a solute divided by the voltune of the solution. Therefore, <br />the expected concentration of sulfate in the backfilled pit should be approximately: <br />' 1.45E + 9 g SO4 _ <br />8.88E + 5 m3 groundwater - 1633 g/m3 SOa. <br />1 <br />A concentration of one g/m' r~ a concentration of one mg/L, so the maximum <br />' "expected" concentration would be about 1600 mg/L 504. The observed concentration <br />in BF-2 in early October 1998 was 1370 mg/L. Given that the analytical precision of <br />sulfate analyses at these levels is about ± 10% (ls), the estimated and observed values <br />' are essentially indistinguishable. <br />' Therefore, the observed available data on TDS and sulfate in BF-2 can be explained <br />fully by the leachability of sulfate as "wash off" from gneiss in the West Pit backfill. <br />Analysis of the solution chemistry from BF-2 using standard computer speciation codes <br />(e.g., PHREEQCI, using the WATEQ4F database) indicates that the solution is <br />saturated with both calcite and gypsum (Attachment 1). Therefore, the sulfate and <br />' calcium concentrations will not rise discernibly above those currently observed because <br />the addition of either or both would cause additional gypsum to form, bufferiAg the Ca <br />and SOa concentrations. Because sulfate and calcium constitute 88 percent of the <br />' Geochimica, Inc. lt~Nov-98 <br />