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Experimental study of acidity-consuming processes in mining waste rock: some influences of mineralogy and particle size
Institution:1. Royal Institute of Technology, Department of Chemistry, Inorganic Chemistry, S-100 44 Stockholm, Sweden;2. University of Sheffield, Department of Civil and Structural Engineering, Mappin Street, Sheffield, S1 3JD, UK;1. Petrolab Limited, C Edwards Offices, Gweal Pawl, Redruth, Cornwall TR15 3AE, United Kingdom;2. SRK Consulting (UK) Ltd, 5th Floor, Churchill House, 17 Churchill Way, Cardiff CF10 2HH, United Kingdom;3. SRK Consulting US Inc., Suite 300, 5250 Neil Road, Reno, NV 89502, USA;4. Geochemic Ltd, Abergavenny, Wales, United Kingdom;1. Department of Geological Sciences and Geological Engineering, Queen’s University, Kingston Ontario, Canada;2. Nexa Resources, Engenheiro Luís Carlos Berrini Avenue 105, 6 floor, Itaim Bibi 04.571-010, São Paulo, SP, Brazil;3. Robert M. Buchan Department of Mining, Queen’s University, Kingston, Ontario, Canada
Abstract:Weathering reactions producing and consuming acid in fresh waste rock samples from the Aitik Cu mine in northern Sweden have been investigated. Batch-scale (0.15 kg) acid titrations with waste rock of different particle sizes were operated for 5 months. The pH was adjusted to a nearly constant level, similar to that in effluents from waste rock dumps at the site (pH near 3.5). The reactions were followed by analysing for all major dissolved elements (K, Na, Mg, Ca, Si, Al, SO4, Cu, Zn, Fe) in aliquots of solution from the reaction vessels. In addition, the solids were physically and chemically characterised in terms of mineralogy, chemical composition, particle size distribution, surface area and porosity. The results show that the alkalinity production is initially dominated by a rapid dissolution of small amounts of calcite and rapidly exchangeable base cations on silicate surfaces. Steady-state dissolution of primary silicate minerals also generates alkalinity. The total alkalinity is nearly balanced by input of acid from the steady-state oxidation of sulphides, such that the pH 3.1–3.4 can be maintained without external input of acid or base. There is a large difference in weathering rates between fine materials and larger waste rock particles (diameters (d) >0.25 mm) for both sulphides and silicates. As a result particles with d smaller than 0.25 mm contribute to approximately 80% of the sulphide and silicate dissolution. Calcite dissolution can initially maintain a neutral pH but with time becomes limited by intra-particle diffusion. Calcite within particles larger than 5–10 mm reacts too slowly to neutralise the acid produced from sulphides.
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