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bottom area collected during three sampling events in April,October and December 1996. The <br /> samples were collected from a boat or from the frozen pond surface with a W ildco dredge sampler. <br /> e� <br /> Solids and=ompanying water were placed in five gallon buckets and transported to the lab for <br /> analysis. All analytical work was performed at the facilities of ACZ laboratories, Inc. in <br /> Steamboat Springs,CO. <br /> -i".•• Determination of percent solids was not performed since the method of sample collection made <br /> this analysis somewhat arbitrary. Samples were air dried prior to analysis for total metals. <br /> Samples were digested by microwave techniques in nitric acid and_Ihen analyzed by inductively <br /> '(. .' coupled plasma spectroscopy(ICP,EPA M6010). Aluminum,calcium,iron,manganese and zinc <br /> were determined in this manner. <br /> X-ray diffraction(XRD)analysis was performed on all samples by R.Corbett at the Cyprus <br /> Miami mineralogical facility,Claypool,AZ. Small representative splits of each sample were <br /> pulverized by hand with an agate mortar and pestle to provide minus 270-mesh material for <br /> analysis. Powders were packed in bulk sample holders and were scanned over the range 20=3- <br /> .. / / 75' with CuKa radiation. Tha resulting XRD patterns were interpreted by a combination of • <br /> computer and manual methods. Relative peak intensities were used to make semi-quantitative <br /> �,. abundance estimates. The lower limit of the XRD technique to resolve trace mineral phases is <br /> approximately J percent. The technique is unable to distinguish poorly crystalline or amorphous <br /> phases. <br /> ,� r .S Electron microscopy was performed by D.R.Brosnahan at the Barrick Goldstrike Mine facility <br /> j near Elko,NV using a JEOL 733 wavelength dispersive microprobe. Accelerating voltage was <br /> 25kV,sample current was JOnA and beam diameter was I km. Additional XRD scans were also <br /> performed at these facilities. <br /> •, „�- ggtt�=i, 4 CHARACTERIZATION OF SLUDGE SAMPLES <br /> The chemical,mineralogical and textural characteristics of the four samples were determined by <br /> various analytical techniques. These characteristics are important variables, and aid in the <br /> f interpretation of the leaching data,which is discussed in the companion paper. <br /> \ <br /> 4.1 Mnemlogical composition by XRD <br /> d The mineralogical composition of the sludge samples,as determined by XRD,is summarized in <br /> i� 9 Table I and Figures 3 and 4(Corbett 1997;Brosnehan 1997). Samples fall into two types;those <br /> dominated by a detrital component from the underlying failings(samples from 3-dam and 5-dam) • <br /> and those dominated water treatment products(samples from the delta and 6-riser). The two <br /> 7 p <br /> samples with large derital components we primarily composed of quartz and muscovite,with <br /> minor potassium feldspar (orthoclase), albite and calcite, with trace kaolinite, gypsum and <br /> !1`. "( 6 r. Q1 ' molybdenite. These samples contain a small sludge component, reflected by the presence of <br /> i 1 ;a t: • gypsum and calcite, since these minerals are uncommon in the Climax orebody. The total <br /> p unidentified portion of these sam les was estimated at 3-10 percent. The low background counts <br /> on these scans indicate there is little amorphous material. <br /> Samples with a large sludge component are dominated by the hydrated calcium-aluminum <br /> Q Q Q ) sulfate hydroxide mineral ettringile(Cat lr(SOr),(OH)jr•26HtO),with minor calcite,fluorite,and <br /> Irace to minor quartz. Calcite appears to be more abundant in the 6-riser sample. The total <br /> unidentified component was estimated at 3-10 percent. Higher background and broad peaks in the <br /> 6-riser and delta sears indicate that at least some of the sample is corn p posed of amorphous or <br /> poorly crystalline material. <br /> Figure 2. Detailed plan map of the Mayflower pond,illustrating sample locations for this study. <br /> 648 649 <br />