TY - JOUR
T1 - Passivation of pyrite for reduced rates of acid and metalliferous drainage using readily available mineralogic and organic carbon resources
T2 - A laboratory mine waste study
AU - Fan, Rong
AU - Qian, Gujie
AU - Short, Michael D.
AU - Schumann, Russell C.
AU - Brienne, Stephane
AU - Smart, Roger St C.
AU - Gerson, Andrea R.
PY - 2021/12
Y1 - 2021/12
N2 - Acid and metalliferous drainage (AMD) is a major environmental issue resulting largely from exposure to weathering of mine wastes containing pyrite (FeS2). At-source strategies to reduce the rate of formation of AMD have potential to be more cost-effective and sustainable than post-generation downstream treatments. The objective of this study was to examine the efficacy of geochemical and microbial treatments for at-source control through pyrite surface passivation. Six kinetic leach columns (KLCs), using a mine waste containing 3.8 wt% pyrite, were subjected to various treatments: 1) untreated, 2) blended calcite, and applications of 3) calcite-saturated water, 4) lime-saturated water followed by calcite-saturated water, 5) biosolids extract water (providing a source of organic carbon to promote microbial growth) and 6) biosolids extract in calcite-saturated water. The untreated KLC leachate pH was on average 5.7 for the first 12 weeks, followed by a gradual decrease to pH 4.5 at week 52. This slow pH decrease is attributed to neutralisation released upon Mg-siderite dissolution. The leachate pH from all treated KLCs was near-neutral at the end of the tests. Pyrite was surface-passivated and leaching supressed by all treatments except for calcite-saturated water. Leaching of Mn and Zn from the untreated waste identified the potential for adverse environmental impact. No evidence was found for surface passivation of Zn- or Mn-containing minerals in the treated KLCs. Blended calcite addition and lime-saturated water followed by calcite-saturated water were most effective at reducing release of Zn and Mn, likely due to precipitation as hydroxides/carbonates.
AB - Acid and metalliferous drainage (AMD) is a major environmental issue resulting largely from exposure to weathering of mine wastes containing pyrite (FeS2). At-source strategies to reduce the rate of formation of AMD have potential to be more cost-effective and sustainable than post-generation downstream treatments. The objective of this study was to examine the efficacy of geochemical and microbial treatments for at-source control through pyrite surface passivation. Six kinetic leach columns (KLCs), using a mine waste containing 3.8 wt% pyrite, were subjected to various treatments: 1) untreated, 2) blended calcite, and applications of 3) calcite-saturated water, 4) lime-saturated water followed by calcite-saturated water, 5) biosolids extract water (providing a source of organic carbon to promote microbial growth) and 6) biosolids extract in calcite-saturated water. The untreated KLC leachate pH was on average 5.7 for the first 12 weeks, followed by a gradual decrease to pH 4.5 at week 52. This slow pH decrease is attributed to neutralisation released upon Mg-siderite dissolution. The leachate pH from all treated KLCs was near-neutral at the end of the tests. Pyrite was surface-passivated and leaching supressed by all treatments except for calcite-saturated water. Leaching of Mn and Zn from the untreated waste identified the potential for adverse environmental impact. No evidence was found for surface passivation of Zn- or Mn-containing minerals in the treated KLCs. Blended calcite addition and lime-saturated water followed by calcite-saturated water were most effective at reducing release of Zn and Mn, likely due to precipitation as hydroxides/carbonates.
KW - Acid drainage
KW - Geochemical remediation
KW - Metalliferous drainage
KW - Microbial remediation
KW - Pyrite passivation
UR - http://www.scopus.com/inward/record.url?scp=85109463291&partnerID=8YFLogxK
UR - http://purl.org/au-research/grants/ARC/LP140100399
UR - http://purl.org/au-research/grants/ARC/LP130100568
U2 - 10.1016/j.chemosphere.2021.131330
DO - 10.1016/j.chemosphere.2021.131330
M3 - Article
AN - SCOPUS:85109463291
SN - 0045-6535
VL - 285
JO - Chemosphere
JF - Chemosphere
M1 - 131330
ER -