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ARCHIVED REPORTS XR0000697
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2900 - Site Mitigation Program
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ARCHIVED REPORTS XR0000697
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Last modified
2/15/2019 7:15:49 PM
Creation date
2/15/2019 4:15:02 PM
Metadata
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Template:
EHD - Public
ProgramCode
2900 - Site Mitigation Program
File Section
ARCHIVED REPORTS
FileName_PostFix
XR0000697
RECORD_ID
PR0522496
PE
2957
FACILITY_ID
FA0015317
FACILITY_NAME
FLAG CITY CHEVRON
STREET_NUMBER
6421
STREET_NAME
CAPITOL
STREET_TYPE
AVE
City
LODI
Zip
95245
APN
05532024
CURRENT_STATUS
02
SITE_LOCATION
6421 CAPITOL AVE
P_LOCATION
99
P_DISTRICT
004
QC Status
Approved
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EHD - Public
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RISC User's Manual Version 4.0 <br /> R=1 f p�d for inorganic chemicals (B-2b) <br /> where <br /> Foy = fraction organic carbon in dry soil [g oc/g soil] <br /> Ko, = organic carbon normalized partition coefficient [ml/g or <br /> m3/kg] <br /> Kd = inorganic distribution coefficient[ml/g] <br /> pb = soil bulk density of the saturated zone [g/cm3] <br /> 0 = porosity(effective)of the saturated zone [cm3/cm3] <br /> If a non-zero value for Kd is entered in the RISC chemical database, the code uses <br /> equation B-2b For organic chemicals that do not have Kd values the code assumes <br /> that the only process causing retardation is the sorption of the chemical due to the <br /> presence of organic carbon in the aquifer In this situation, the quantity Ko,*Fo, is <br /> used to estimate the distribution coefficient (Kd) In reality there may be several <br /> processes (such as the presence of silts and clays) contributing to the retardation (or <br /> . sorption) of the chemical The equations in RISC (and most fate and transport <br /> models)assume that the retardation can be completely predicted using the relationship <br /> in Equation B-2a This will usually under-predict the amount of sorption (and hence <br /> retardation) that is actually occurring Usually this will be conservative for purposes <br /> of estimating risk If it appears that there may be much more retardation occurring <br /> than what the site-specific measured value of Fo,would indicate (usually the case for <br /> low F,soils), the actual partitioning may be measured in a lab and then the measured <br /> Kd value could be entered for the chemical being modeled <br /> This retardation equation assumes that sorption and desorption processes are <br /> instantaneous and fully reversible See Chapter 11 (the chemical database) for <br /> equations for estimating KoG from other chemical parameters <br /> B.2 3 Dispersion Coefficients;w`",� i <br /> The dispersion coefficients in equation B-1 are calculated using the following <br /> relationships <br /> B-4 <br />
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