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2009-08-10_GENERAL DOCUMENTS - M1977300 (3)
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2009-08-10_GENERAL DOCUMENTS - M1977300 (3)
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Last modified
8/24/2016 3:49:32 PM
Creation date
8/13/2009 8:39:00 AM
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DRMS Permit Index
Permit No
M1977300
IBM Index Class Name
GENERAL DOCUMENTS
Doc Date
8/10/2009
Doc Name
EPP- Pgs. 11-53 to 20-1
From
Whetstone Associates/Cotter Corp.
To
DRMS
Permit Index Doc Type
Gen. Correspondence
Email Name
DB2
Media Type
D
Archive
No
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Environmental Protection Plan, Schwartzwalder Mine 14-8 <br />• composition (Ca, SO4, HCOO of the deep mine water is controlled by precipitation and dissolution <br />reactions involving carbonate minerals and gypsum. Ferrihydrite, a mineral that commonly limits iron <br />concentrations in oxidized waters was also calculated as being oversaturated in solution. This result, <br />however, is a statistical artifact of the high detection limit for iron (<0.03 mg/L) that was used to calculate <br />the input value. All uranium and molybdenum minerals evaluated by the model were undersaturated in the <br />deep mine water. <br />Table 146, Controlling Mineral Phases in Deep Mine Water <br />Mineral Composition Saturation Index' <br />Calcite CaC03 0.87 <br />Alunite KA13(S04 2(OH)6 -0.35 <br />Chrome Hydroxide am Cr(OH)3 0.46 <br />Ferrih drite Fe OH)3 1.71 <br />Gypsum CaSO4.2H2O 0.78 <br />M Cr204 MgCr204 -0.34 <br />Ma esite M COs 0.31 <br />Jarosite K KFe3(SO4)2(OH)6 0.36 <br />Otavite CdC03 -0.89 <br />Rhodochrosite MnC03 -0.74 <br />Positive values are oversaturated; negative values are undersaturated <br />(iii). 1.3 Reflooded Mine Water Speciation <br />Speciation runs were performed for four samples collected from the flooded mine. The modeled samples <br />• included, water from a depth of 221 feet collected on May 21, 2001, water from a depth of 465 feet <br />collected on April 18, 2002, water from a depth of 291 feet collected on May 20, 2003, and water from just <br />below the surface on June 27, 2007. The modeled water chemistries had acceptable charge balance errors <br />ranging from -2.46% to 2.52 %. The model calculations for the 2001, 2002, and 2003 samples were <br />performed for oxidizing conditions at an Eh of 178 mV similar to values observed in the flooded mine <br />during that period. The calculations for 2007 were performed using an Eh of 23 mV as was observed <br />during measurements in November 2007. Results of the analysis indicate that calcite and gypsum are near <br />equilibrium for all of the samples and that they are the probable mineral controls of calcium, sulfate and <br />bicarbonate in solution. Amorphous aluminum hydroxide, magnesite, and rhodocrosite were also <br />calculated to be near equilibrium. C02 gas is oversaturated in the mine water as compared to equilibrium <br />with atmospheric pressure (atmospheric equilibrium for C02 gas occurs at saturation indices between -3.2 <br />and -3.5). Ferrihydrite saturation ranges from near equilibrium to oversaturated, but the model results are <br />impacted by the relatively high detection limit for iron (<0.03 mg/L) that was used to calculate the input <br />value. The precipitation of ferrihydrite typically limits iron concentrations in oxidized waters at neutral pH, <br />and is the most probable control limiting iron concentrations in mine water. All of the uranium and <br />molybdenum minerals evaluated by the model were undersaturated in solution. Saturation Indices for the <br />probable controlling phases are presented in Table 14-7. <br />4109C.090807 WhetstoneAssociates
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