Structural-?hemi??l Transformations of Minerals at Mechanical Activation and Their Role in Technological Processes (on the Example of ??ssiterite)

"It has been shown on the example of cassiterite that grinding in mills of the increased power lead to destruction of the fine crystal structure and consequently to change in physical and chemical properties of the mineral, that is its transition into mechanically activated state. The increase in mineral reactivity is related to both the growth of mineral specific surface and sharp decrease in the sizes of primary crystallites accompanied by essential increase in number of microdefects that is clearly expressed in its increasing solubility during interaction with corrosive mediums, especially with acids. Calorimetric measurements indicate that the thermal effect of SnO2 solubility increases considerably.These observations allow us to propose two techniques of hydrometallurgical treatment of cassiterite: direct dissolution of the mechanically activated mineral in acids, although it is a very power-consuming process, and mechanical activation of cassiterite in presence of metals that are able to release hydrogen from acids. Active hydrogen is released during interaction between the mechanical mixture of SnO2 and metal with acids and reduces tin from the mineral transferring it into solution.In addition to other technological properties, the flotability of cassiterite has been thoroughly studied. It has been found that it steadily decreases as activation proceeds because of increase in the degree of hydratability of particle’s surface. In this case, the mechanical activation is provided through tribotreatment of a surface rather than through fine grinding. On this basis we developed the technique of inverse cassiterite flotation with its subsequent transfer into a chamber product that considerably increase the quality of a tin concentrate.The observed technological effects may be generally explained by occurrence of the valenceundersaturated, strained (deformed) chemical bonds and other active centers on the cassiterite surface while decrease in its flotability - by formation of the hydrolyzed tin species and impurity iron, such as Sn(??)4°, Fe(??)2 +, Fe(??)3° hydroxocomplexes and others."