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The chemistry of conventional and alternative treatment systems for the neutralization of acid mine
Science of the Total Environment 366 (2006) 395–408
/locate/scitotenvReview
The chemistry of conventional and alternative treatment systems for
the neutralization of acid mine drainage☆
Margarete Kalin ?, Andrew Fyson, William N. Wheeler
Boojum Research Ltd, 139 Amelia Street, Toronto, Ontario, Canada, M4X1E6
Received 13 June 2005; received in revised form 26 October 2005; accepted 1 November 2005Abstract
The oxidation of pyritic mining waste is a self-perpetuating corrosive process which generates acid mine drainage (AMD)
effluent for centuries or longer. The chemical neutralization of these complex, buffered effluents result in unstable, metal-laden
sludges, which require disposal to minimize long-term environmental consequences. A variety of passive treatment systems for
AMD, developed in the past two decades, combine limestone and organic substrates in constructed wetlands. These systems work
well initially but over the longer term fail due to clogging with and the depletion of available organic carbon. However, some
ecologically engineered systems, which exploit the activities of acid reducing microbes in the sediment, rely on photosynthesis in
the water column as a source of organic matter. The primary productivity in the water column, which also generates some
alkalinity, provides electron donors for the microbial reduction processes in the sediment. In its consideration of ‘passive’ systems,
the literature has placed undue emphasis on sulphate reduction; thermodynamical iron reduction is equally important as is the need
to prevent iron oxidation. Secondary precipitates of iron play a significant role in sediment-driven biomineralization processes,
which affect the anaerobic degradation of organic matter and the stability of the resulting metal sulfides. One such passive system,
which utilized a floating root mass as a source of organic carbon, is described. An extensive review of the literature and the
chemical and biogeochemical reactions of AMD treatment s
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