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Kinetic modelling of geochemical processes at the Aitik mining waste rock site in northern Sweden
Institution:1. Earth and Environmental Systems Institute and Department of Geosciences, The Pennsylvania State University, University Park, PA 16802, USA;2. Department of Earth Sciences, Dickinson College, Carlisle, PA 17013, USA;3. Department of Geological Sciences, University of Texas at El Paso, El Paso, TX 79968, USA;1. New Mexico Institute of Mining and Technology, 801 Leroy Pl., Socorro, New Mexico, USA 87801;2. Kjeøy Research and Education Center, Vestbygd, Norway 8412;3. Mahoney Geochemical Consulting LLC, 892 S Newcombe Way, Lakewood, Colorado, USA 80226
Abstract:A steady-state geochemical model has been developed to study water-rock interactions controlling metal release from waste rock heaps at the Aitik Cu mine in northern Sweden. The Cu release in drainage waters from the site is of environmental concern. The waste rock heaps are treated as single completely mixed flow-through reactors. The geochemical model includes kinetices of sulphide and primary silicate mineral weathering, heterogeneous equilibrium with secondary mineral phases and speciation equilibrium. Field monitoring of drainage water composition provides a basis for evaluation of model performance.The relative rate of oxidative weathering of sulphides and dissolution of primary silicate minerals, using published kinetic data, are consistent with net proton and base cation fluxes at the site. The overall rate of Fe2+ oxidation within the heap is three orders of magnitude faster than that which could be explained by surface-catalysed reaction kinetics. This suggests significant activity of iron-oxidizing bacteria. The absolute weathering rates of sulphides and silicate minerals, normalized to a measured BET surface area, are approximately two orders of magnitude lower at field scale than published rates from laboratory experiments. Because of the relative absence of carbonate minerals, the weathering of biotite and plagioclase feldspar are important sources of alkalinity.
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