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Groundwater Concentrations Under a Worst Case Scenario <br /> As a worst-case estimate, the groundwater concentration of chromium was calculated assuming 100% <br /> of the metal in the sediments was transported into the groundwater (Table 3) The result of this <br /> calculation depends on the volume of water into which the metal is placed If it is assumed that all the <br /> metal moves into aquifer pores and dilution effects from groundwater flow are neglected, high <br /> groundwater metal concentrations result because of the aquifer's high solid to water ratio For <br /> comparison, Table 3 also shows the chromium groundwater concentration that would result if <br /> chromium in sediments at the ESL level were transferred into aquifer pores <br /> As shown by the high metal concentrations trations listed in Table 3, it is extremely unrealistic to assume that <br /> all of the chromium in the aquifer sediments will dissolve into the groundwater during ozone treatment <br /> Metals may be physically bound inside sediment particles or occur as mineral forms resistant to ozone <br /> oxidation At present, there is no basis for selecting what fraction, if any, of the sediment chromium <br /> would be mobilized by ozone treatment As noted earlier, a bench scale study of ozone reaction with <br /> aquifer sediments from the gasoline impacted zone would help predict the extent of metal mobilization <br /> during ozone treatment <br /> Geochemical Factors that Affect Water Quality and the Success of Ozone Treatment <br /> Water quality may be affected by ozone treatment This effect would be greatest if the aquifer were <br /> highly anaerobic, that is, methanogenic or sulfate reducing In this case, oxidation of reduced iron and <br /> manganese in the groundwater could lead to formation of insoluble iron oxide and manganese oxide <br /> particles that could conceivably affect aquifer hydraulic properties If sulfide minerals or dissolved <br /> hydrogen sulfide were oxidized, groundwater sulfate levels would rise increasing the overall dissolved <br /> solids in the groundwater Oxidation processes themselves generally release protons decreasing <br /> aquifer pH, although, Crimi et al (2003) reported both pH decreases and increases in different <br /> sediments treated with permanganate. Dissolution of carbonate and other minerals if present-in <br /> aquifer sediment may react with acidity produced by ozone treatment, helping to prevent a drop in pH <br /> Water extracts of aquifer solids contained 23 mg/L alkalinity reported as calcium carbonate (CaCO3) <br /> Assuming that all the pH buffering capacity in the aquifer is derived from groundwater alkalinity and <br /> from the water extractable alkalinity in the solid phase and assuming all the alkalinity measured in soil <br /> extracts from MW-9R is present in the solids as CaGO3, the aquifer could neutralize approximately <br /> 2,000 mEq/m3 aquifer from groundwater alkalinity and approximately 9,000 mEq/m3 aquifer from water <br /> extractable solid-phase alkalinity These calculations assume an aquifer porosity of 0 3 and a particle <br /> density of 2 65 g/cm3 A bench scale study, using materials from the gasoline impacted area, may <br /> help elucidate the actual changes in water quajity that could occur under ozone treatment <br /> Ozone will be consumed by the "reduction capacity" of the aquifer, lowering the ability of the oxidation <br /> treatment to remove target compounds -For-our-purposes,-the relevant-aquifer reduction-capacity is the -- -- <br /> G�Oocuments and 4 <br /> SetOngslcrtohnsonNr)osktop\Unocal\GeochemEvat—D November 2004 <br /> oc doc <br />