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2013 Semiannual Groundwater Monitoring and Evaluation Report <br /> Full-Scale In Situ Hexavalent Chromium Reduction Treatment Implementation <br /> Former Marley Cooling Tower Site,Stockton,California August 2013 <br /> • The polysulfide reduces ferric oxyhydroxide coatings on aquifer solids, converting the <br /> ferric ion to the more mobile ferrous iron. <br /> • A portion of the ferrous iron migrates with moving ground water, and reacts with <br /> dissolved hexavalent chromium in the ground water. <br /> • A portion of the ferrous iron forms ferrous minerals which sorb onto the aquifer solids <br /> and thus form a borehole-placed reactive barrier(Rouse et al., 2006), available to react <br /> with and reduce hexavalent chromium dissolved in ground water passing the sorption <br /> site. <br /> During the Phase 1 of the pilot test, it was documented that this sorbed ferrous iron is capable of <br /> exerting reduction for at least two years, in a portion of the aquifer with high dissolved <br /> hexavalent chromium concentration. Thus, while calcium polysulfide is a liquid and able to <br /> migrate through an aquifer, upon entry into an aquifer environment, much of the reductive <br /> capacity becomes fixed in place within the original radius of impact of the pressure injection. In <br /> the case of the horizontal injections, the injections would form a `floor' under the retort pit, with <br /> the capacity to reduce high concentrations of hexavalent chromium being displaced by shallow <br /> input of water, but it might not be able to migrate below the point of injection due to <br /> consumption by oxygen present in the vadose zone pore space. <br /> In May 2009, the CVRWQCB approved, by electronic mail, a program modification proposal to <br /> discontinue nitrate analyses as part of the in situ RAP Amendment activities (CVRWQCB, <br /> 2009). This change to the sampling program was incorporated into the third quarter of 2009 and <br /> subsequent sampling events. <br /> (a MWK, <br /> 2-3 <br />