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   <subfield code="a">Inhibition of Acid Mine Drainage from a Pyrite-rich Mining Waste Using Industrial By-products: Role of Neo-formed Phases</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[P. Sahoo, S. Tripathy, M. Panigrahi, Sk. Equeenuddin]</subfield>
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   <subfield code="a">In the present study, the potential use of the industrial waste residues, such as coal fly ash and clinker dust, was evaluated in inhibiting acid mine drainage generation from pyrite-rich wastes using non-saturated column experiments. Two columns (B and C) were filled with a mixture of industrial residues over pyrite-quartz sand (PS), while one column (A) used as the control was solely filled with PS. Artificial irrigation was maintained in each column by pouring Milli-Q water (pH 6.5). The leachate chemistry and the precipitation of neo-formed phases in the columns were examined. Based on the pH and concentration of SO4 2− in the effluent collected over a period of time, it can be inferred that pyrite dissolution was dominant in column A. In columns B and C, the addition of industrial waste produced a near neutral to alkaline leachate. At this pH, Fe released from pyrite oxidation was immediately depleted by precipitating into Fe-oxyhydroxide phases that likely coated the pyrite grains (termed as microencapsulation) which inhibited oxidation. This was supported from the scanning electron microscope observation and the geochemical modeling results. In addition, the precipitation of other neo-formed phases such as calcium carbonate and gypsum, along with the pozzolanic reactions of industrial wastes, possibly increased the cementation of fly ash particles leading to the development of a compact material, which prevented further oxidation by restricting infiltration and oxygen contact to the pyrite surface. This occurred best in column B; thus, it produced better quality of leachates than column C, though at the end both columns showed a significantly decreased concentration of Fe (up to 99.9%) and other metals such as Cu, Cr, Pb, Zn, and Mn (lower values than the WHO permissible limits of drinking water) compared to control.</subfield>
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   <subfield code="u">Vale Institute of Technology Sustainable Development, Boaventura da Silva, 66055-090, Belém, Pará, Brazil</subfield>
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   <subfield code="u">Department of Geology &amp; Geophysics, Indian Institute of Technology, 721302, Kharagpur, West Bengal, India</subfield>
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   <subfield code="u">Department of Mining Engineering, National Institute of Technology, 769008, Rourkela, Odisha, India</subfield>
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