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FIELD DOCUMENTS_1982-1985
EnvironmentalHealth
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EHD Program Facility Records by Street Name
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W
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WAGNER
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200
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2900 - Site Mitigation Program
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PR0009002
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FIELD DOCUMENTS_1982-1985
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Last modified
6/17/2020 3:05:54 PM
Creation date
6/17/2020 1:48:37 PM
Metadata
Fields
Template:
EHD - Public
ProgramCode
2900 - Site Mitigation Program
File Section
FIELD DOCUMENTS
FileName_PostFix
1982-1985
RECORD_ID
PR0009002
PE
2960
FACILITY_ID
FA0004040
FACILITY_NAME
SPX COOLING TECHNOLOGIES INC
STREET_NUMBER
200
Direction
N
STREET_NAME
WAGNER
STREET_TYPE
AVE
City
STOCKTON
Zip
95215
APN
14331007
CURRENT_STATUS
02
SITE_LOCATION
200 N WAGNER AVE
P_LOCATION
99
P_DISTRICT
002
QC Status
Approved
Scanner
LSauers
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EHD - Public
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A2 <br /> ( The geochemical processes involved are extremely dynamic. Some <br /> ` processes tend to remove contaminants , while others exchange one <br /> contaminant for the other, or actually may add contaminants to <br /> the system. As an acidic plume advances downgradient, reactions <br /> may take place that will alternately remove and redissolve <br /> contaminants . Understanding of such processes is required to <br /> analyze the observed water-quality data and to plan for remedial <br /> measures. Each of the following described processes appear to be <br /> important in considering the environmental impacts of acidic <br /> plumes moving downgradient from acid uranium mill tailings ponds <br /> or evaporation ponds. <br /> I By far the single most significant geochemical reaction is that <br /> of calcite dissolution, wherein the hydrogen ions react with <br /> calcite or other carbonate material present in the soil or rock. <br /> The mechanism is calcite reacting with hydrogen ion to liberate <br /> calcium ion and form bicarbonate ion . This results in the <br /> gradual downgradient movement of an acidic reaction front, and an <br /> acid-front retardation in the saturated zone , relative to the <br /> rate of water travel . Hydrogen ions in the acidic plume are <br /> consumed by calcite dissolution. The retardation of the advance <br /> of the acid front is a result of the number of pore volumes of <br /> water with specified hydrogen ion concentration that must react <br /> jwith a representative volume of the porous media to completely <br /> remove the total mass of calcite in the volume (Cherry, Shepherd, <br /> t <br /> i <br />
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