Page 177 - Introduction to Mineral Exploration
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160   C.J. MOON



                  and it is not desirable to operate two number-  65°C so that volatile elements such as mercury
                  ing systems, so some arrangement should be  are not lost. Drying is generally followed by
                  made with the laboratories to randomize the  gentle disaggregation and sieving to obtain
                  samples within an analytical batch. The results  the desired size fraction. Care should be taken
                  can then easily be re-sorted by computer.   to avoid the use of metallic materials and to
                    When laboratory results become available  avoid carryover from highly mineralized to
                  the data should be plotted batch by batch to  background samples. Preparation of rocks and
                  examine the within- and between-batch effects.  vegetation is usually carried out in the labor-
                  The effects observable within a batch are pre-  atory and care should be taken in the selec-
                  cision and systematic instrumental drift. Pre-  tion of crushing materials. For example, in a
                  cision should be monitored by calculating the  rock geochemical program a company search-
                  average and difference between duplicates on a  ing for volcanic-associated massive sulfides
                  chart such as is detailed by Thompson (1982).  found manganese anomalies associated with
                  The precision for most applications should be  a hard amphibolite. They were encouraged by
                  less than about 20%, although older methods  this and took it as a sign of exhalative activity.
                  may reach 50%. If precision is worse than anti-  Unfortunately further work showed that the
                  cipated then the batch should be re-analyzed.  manganese highs were related to pieces of man-
                  Systematic drift can be monitored from the  ganese steel breaking off the jaw crusher and
                  reference materials within a batch and the  contaminating the amphibolite samples. Other
                  reagent blanks. Between-batch effects represent  less systematic variation can be caused by
                  the deviation from the expected value of the  carryover from high grade samples, for example
                  reference material and should be monitored by  not cleaning small grains of mineralized vein
                  control charts. Any batch with results from ref-  material (e.g. 100,000 ppb Au) will cause signi-
                  erence materials outside the mean ±2 standard  ficant anomalies when mixed with background
                  deviations should be re-analyzed; commercial  (1 ppb Au) rock. Contamination can be elimin-
                  laboratories normally do this at no further  ated by cleaning crushing equipment thor-
                  charge. Long-term monitoring of drift can show  oughly between samples and by checking this
                  some interesting effects. Coope (1991) was able  by analyzing materials such as silica sand.
                  to demonstrate the disruption caused by the   The Bre-X scandal, in which alluvial gold
                  moving of laboratories in a study of the gold ref-  was added to drill pulps before sending the
                  erence materials used by Newmont Gold Inc.  samples for analysis (see section 5.4), empha-
                                                              sizes the importance of recording the methods
                                                              of sample preparation and controlling access to
                  8.2.2 Sample collection and preparation
                                                              the samples.
                  Samples should be collected in nonmetallic
                  containers to avoid contamination. Kraft paper
                  bags are best suited for sampling soils and  8.2.3 Analytical methods
                  stream sediments because the bags retain their  Most analysis is aimed at the determination of
                  strength if the samples are wet and the samples  the elemental concentrations in a sample and
                  can be oven dried without removing them from  usually of trace metals. At present it is impos-
                  their bags. Thick gauge plastic or cloth are pre-  sible to analyze all elements simultaneously
                  ferred for rock samples. All samples should be  at the required levels, so some compromises
                  clearly labeled by pens containing nonmetallic  have to be made (Fig. 8.3). In exploration for
                  ink.                                        base metals it is usual to analyze for the ele-
                    Most sample preparation is carried out in the  ments sought, e.g. copper in the case of a copper
                  field, particularly when it involves the collec-  deposit, and as many useful elements as pos-
                  tion of soils and stream sediments. The aim of  sible at a limited extra cost. With modern tech-
                  the sample preparation is to reduce the bulk of  niques it is often possible to get 20–30 extra
                  the samples and prepare them for shipment.  elements, including some that provide little
                  Soils and stream sediments are generally dried  extra information but a lot of extra data for in-
                  either in the sun, in low temperature ovens, or  terpretation. The major methods are as shown
                  freeze dried; the temperature should be below  in Table 8.3 but for detail on the methods used
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