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Results from a reconnaissance scale heavy mineral ... - arkisto.gsf.fi

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Lehtonen et al.<br />

<strong>Results</strong> <strong>from</strong> a <strong>reconnaissance</strong> <strong>scale</strong> <strong>heavy</strong> <strong>mineral</strong> survey of kimberlitic indicator <strong>mineral</strong>s…<br />

tored by processing of blank till samples each spiked with 0.25–0.5 mm fraction Cr-pyrope<br />

grains (Lehtonen and Marmo, 2002). The preconcentration process reduced the till samples to<br />

700–1000 g. Final <strong>heavy</strong> <strong>mineral</strong> concentrates were liberated by <strong>heavy</strong> medium separation<br />

(HMS) using methylene iodine (d =3.3 gcm -3 ). A dry low intensity drum magnetic separator<br />

(LIMS) was applied to the HMS concentrates to remove magnetite. Finally, the 0.25–1.0 mm<br />

size indicator grains were hand picked under binocular microscope <strong>from</strong> the non-magnetic fraction.<br />

In order to con<strong>fi</strong>rm optical identi<strong>fi</strong>cation, all indicator grains were analyzed using an EDS<br />

equipped Jeol JSM-5900LV scanning electron microscope. Quantitative <strong>mineral</strong> compositions<br />

<strong>from</strong> selected indicator grains were determined by Cameca Camebax SX50 and SX100 electron<br />

microprobes. For garnet, ilmenite and chromite analyses, an acceleration voltage of 25 kV, probe<br />

current of 48 nA (or 55 nA) and beam diameter of 1 µm were applied. The parameters for clinopyroxene<br />

analyses were 15 kV, 30 nA and 5 µm, respectively. A simpli<strong>fi</strong>ed schematic flow sheet<br />

for sample processing is presented in Figure 2.<br />

>1 mm<br />

Optical microscopy<br />

or stored<br />

Overflow<br />

stored<br />

d < 3.3<br />

stored<br />

Magnetic fraction<br />

stored<br />

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