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Workplan for Vertical Groundwater Investigation <br /> And Bench Test for In-Situ Oxidation <br /> 7835 Thornton Road, Stockton, CA <br /> Page 6 of 8 <br /> extraction would have limited effect on the sorbed contaminant mass, whereas in-situ <br /> oxidation has a tendency to aid in desorption of contaminants bound to the soil substrate. <br /> This occurs because the hydroxyl radicals created by the oxidation process are non-selective, <br /> and in addition to attacking the target contaminant compounds, they also attack the soil-based <br /> organic matter that binds the contaminants to the soil. <br /> We propose to evaluate in-situ oxidation using a modified Fenton's Reagent as the oxidizing <br /> solution. Fenton's Reagent has long been used in the wastewater treatment industry. In <br /> government-sponsored studies, the in-situ injection of Fenton's Reagent has been shown to be <br /> effective in oxidizing organic contaminants such as fuel hydrocarbons and chlorinated solvents. <br /> Fenton's Reagent is one of strongest oxidizers known due to the formation of hydroxyl radicals <br /> by the catalysis of hydrogen peroxide. Classic Fenton's Reagent consists of a solution of H2O2 <br /> catalyzed by iron, typically in the form of FeSO4. The oxidizing strength of the solution is <br /> maximized when the treated water is at a pH of approximately 3-5. This is typically <br /> accomplished by the addition of sulfuric acid (which is a common adulterant of commercial- <br /> grade FeSO4). Temperature will rise with the reaction. The optimal temperature is between 70- <br /> 100° F. To control temperature and pH, it may be necessary to stage the introduction of <br /> peroxide. <br /> Working in conjunction with In-situ Oxidative Technologies, Inc. (ISOTEC), we propose to use a <br /> modified Fenton-based process that has been designed to function at natural subsurface <br /> conditions, with pH — 7.0 and temperature within 10° C of normal. ISOTEC uses patented <br /> reagents designed for neutral subsurface conditions and efficient hydroxyl radical and superoxide <br /> generation. ISOTEC's oxidation and reduction method utilizes a site-specific delivery system <br /> designed to treat organic contaminants within an area of concern. ISOTEC oxidants and catalysts <br /> react with the organic contaminants within the subsurface producing innocuous by-products such <br /> as carbon dioxide and water. ISOTEC's process utilizes patented chelating agents as the catalyst <br /> for the reaction rather than FeSO4, which tends to limit the leaching of naturally occurring metals <br /> that occurs in the acidified environment of classic Fenton's chemistry. ISOTEC's reagents have <br /> also been designed to increase the mobility of the oxidants by preventing precipitation or fixation <br /> of iron to native soil, thereby promoting its availability for hydroxyl radical generation from <br /> peroxide. <br /> Bench Test <br /> The oxidizing strength of the reagent has the potential to alter the valence of metallic ions and <br /> halogens. The Regional Water Quality Control Board, Central Valley Region (RWQCB) has <br /> expressed particular concern about the possibility of oxidizing trivalent chromium to the more <br /> toxic and mobile hexavalent species and/or oxidizing bromide to the +5 valence state creating the <br /> toxic bromate ion. Consequently, bench testing is required before RWQCB will consider <br /> permitting the injection of oxidizers into contaminated aquifers. Depending upon the results of <br /> the bench testing, injection may be permitted with or without Waste Discharge Requirements, or <br /> may be forbidden altogether. <br /> G:\GROUNDZE\KNOWLES.HAM\REPORTS\WKPLAN_deepwell—bench2.doc <br />