Page 44 - Introduction to Mineral Exploration
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2: MINERALOGY OF ECONOMIC DEPOSITS  27


                 provide a photographic image of the surface.  fundamental parameters used in the design
                 Other electrons penetrate to depths of 1–2 µm  and optimization of processing plants. Gu
                 and excite the atoms of the mineral causing  (2002) explained that the MLA system consists
                 them to give off characteristic X-radiation  of a specially developed software package and a
                 which can be used to identify the elements   standard modern SEM fitted with an energy
                 present and measure their amounts. With this  dispersive spectrum (EDS) analyzer. The
                 chemical information and knowledge of some   on-line program of the MLA software pack-
                 optical properties reasonable inferences can be  age automatically controls the SEM, captures
                 made concerning the identity of minute grains  sample images, performs necessary image ana-
                 and inclusions. In addition important element  lysis (see Chapter 6), and acquires EDS X-ray
                 ratios such as Fe:Ni in pentlandite ((Fe,Ni) 9 S 8 )  spectra. Typically, 40–100 images (containing
                 and Sb:As in tetrahedrite ((Cu,Fe,Ag,Zn) 12 Sb 4 S 13 )  4000–10,000 grains) are acquired for each
                 –tennantite ((Cu, Ag,Fe,Zn) 12 As 4 S 13 ), and small  sample block and a dozen blocks (of 30 mm
                 amounts of possible byproducts and their     diameter) are measured overnight. The MLA
                 mineralogical location can be determined. Use-  off-line processing program transforms the raw
                 ful references are Goldstein et al. (1981), Reed  image into quality sample images, from which
                 (1993), and Zussman (1977).                  most important minerals can be differentiated
                   The ion microprobe uses an ion rather an   using modern image analysis methods.
                 electron source and measures the mass of
                 secondary ions from the sample rather than X-
                 rays. This technique allows the measurement  Differential thermal analysis
                 of much lower concentrations of heavy ele-   This method is principally used for clay and
                 ments than the electron microprobe and has   clay-like minerals which undergo dehydration
                 been widely used in the search for the location  and other changes on heating. Measurement
                 of gold and PGM in metallurgical testing. A  of the differences in temperature between an
                 summary of the technique can be found in     unknown specimen and reference material
                 Larocque and Cabri (1998).                   during heating allow for the determination of
                                                              the position and intensity of exothermic and
                                                              endothermic reactions. Comparison with the
                 Scanning electron microscopy (SEM)
                                                              behavior of known materials aids in the iden-
                 SEM is of great value in the three-dimensional  tification of extremely fine-grained particles
                 examination of surfaces at magnifications from  that are difficult to identify by other methods
                 ×20 to 100,000. Textures and porosity can be  (Hutchison 1974).
                 studied and, with an analytical facility, indi-
                 vidual grains can be analyzed and identified in
                 situ. Excellent microphotographs can be taken  Autoradiography
                 and, with a tilting specimen stage, stereo-  Radioactive minerals emit alpha and beta
                 graphic pairs can be produced. This equipment  particles which can be recorded on photo-
                 is particularly valuable in the study of lime-  graphic film or emulsions in contact with the
                 stones, sandstones, shales, clays, and placer  minerals, thus revealing their location in a rock
                 materials. The method is discussed in Gold-  or ore. In ores this technique often shows up
                 stein et al. (1981) and Tucker (1988). Recent  the presence of ultra-fine-grained radioactive
                 developments such as the QEM (Quantitative   material whose presence might otherwise go
                 Evaluation of Minerals)*SEM allows the auto-  unrecorded. The technique is simple and cheap
                 matic quantification of mineral composition   and suitable for use on hand specimens and
                 and size in a similar manner to point count  thin and polished sections (Robinson 1952,
                 and image analysis for optical microscopes,  Zussman 1977).
                 although the QEM*SEM is rapidly being over-
                 taken by the Mineral Liberation Analyser
                 (MLA) which has particular importance in     Cathodoluminescence
                 applied mineralogy and metallurgical pro-    Luminescence (fluorescence and phosphores-
                 cessing. Mineral Liberation Analyser data are  cence) is common in the mineral kingdom.
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