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ARCHIVED REPORTS_XR0006121
Environmental Health - Public
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ARCHIVED REPORTS_XR0006121
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Last modified
4/10/2020 4:33:57 PM
Creation date
4/10/2020 2:08:36 PM
Metadata
Fields
Template:
EHD - Public
ProgramCode
2900 - Site Mitigation Program
File Section
ARCHIVED REPORTS
FileName_PostFix
XR0006121
RECORD_ID
PR0540885
PE
2960
FACILITY_ID
FA0023381
FACILITY_NAME
FORMER EXXON SERVICE STATION NO 73942
STREET_NUMBER
4444
Direction
N
STREET_NAME
PERSHING
STREET_TYPE
AVE
City
STOCKTON
Zip
95207
APN
11022017
CURRENT_STATUS
01
SITE_LOCATION
4444 N PERSHING AVE
P_LOCATION
01
QC Status
Approved
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EHD - Public
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• <br /> EXECUTIVE SUMMARY <br /> Bench-scale treatability testing was conducted on soil and groundwater from the Exxon <br /> 43942 site in Stockton, California, which contained diesel range total petroleum <br /> hydrocarbons (TPH-d), gasoline range total petroleum hydrocarbons (TPH-g), BTEX <br /> compounds (benzene, toluene, ethylbenzene and xylenes), and methyl-t-butyl ether <br /> (MTBE) Testing was conducted to evaluate and compare the ability of ozone (03) and <br /> Peroxone (a mixture of ozone and hydrogen peroxide) to remove petroleum hydrocarbons <br /> from soil and groundwater at the site and to determine whether removal was due to <br /> volatilization (by sparging) or to destruction (via chemical oxidation) This was <br /> accomplished by comparing the effect of sparging with a chemically inert gas (nitrogen) <br /> to the effect of sparging with ozone The effect of each treatment on hexavalent <br /> chromium [(Cr(VI)] (which can be formed by oxidation of naturally occurring trivalent <br /> chromium) and other secondary water quality parameters were also evaluated The <br /> potential fate of Cr(VI), which was sometimes formed by ozone and Peroxone, was also <br /> assessed <br /> The laboratory study clearly demonstrated that ozone and Peroxone (a mixture of ozone <br /> and hydrogen peroxide) could destroy TPH-g, TPH-d and BTEX in soil and groundwater <br /> from this site Destruction appears to be more efficient with Peroxone, which volatilized <br /> lower amounts of COCs than ozone Sparging with nitrogen (an inert gas) also <br /> . significantly reduced the amount of CDCs in groundwater, but the removal was due to <br /> volatilization, not destruction of hydrocarbons <br /> Treatment with ozone and Peroxone generated Cr(VI), but tests indicate that this Cr(VI) <br /> can naturally attenuate when in contact with untreated soil In some tests, the amount of <br /> Cr(VI) produced was very low (< 6 ttg/L) In other tests, the Cr(VI) was very high (570 <br /> gg/L) The cause of the variability is unknown Tests indicated that untreated soil could <br /> reduce Cr(VI) to its trivalent form, and that the amount of Cr(VI) that can be generated is <br /> significantly less than the amount that untreated soil is capable of reducing <br /> Bromate was not detected above the detection limit of 8 µg/L in either the ozone or <br /> Peroxone tests Although the concentration of bromide decreased in these tests, it was <br /> not converted to bromate <br /> The effect of ozone and Peroxone on most other water quality parameters was small <br /> Exceptions were barium and vanadium, the concentrations of which increased upon <br /> treatment <br /> The groundwater oxidant demand was 110-180 mg 03/L, which is lower than predicted <br /> based on the concentrations of COCs, but indicates that the clean groundwater does not <br /> have an excessively high demand The soil oxidant demand was 400-700 mg 03/kg soil <br /> PRIMA Environmental Eval of Peroxone <br /> June 1,2005 ETIC-Exxon#f3942 <br />
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