“…This approach is often good enough to yield some reasonable results if a priori knowledge of species is assumed based on the matching of chemical elements from elemental analysis; however, this approach fails when the concetration of the phases is below the detection limit of lab based XRD (~ 4-5 w.t.%) or when the sample is not perfecly crystalline in nature. Indeed in our studies (Gomez et al, 2010b(Gomez et al, , 2011c) both scenerios were encountered in the industrial samples analyzed (Dymov et al, 2004;Defreyne et al, 2009;Mayhew et al, 2010;Bruce at al., 2011). For example, in the case of the gold produced residue (Figure 9), although the sample was crystalline in nature, the amount of arsenic (as AsO 4 ) in the solid was ~ 1 w.t.…”