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Conca, J. L., & Wright, J. (2006). An Apatite II permeable reactive barrier to remediate groundwater containing Zn, Pb and Cd. Appl. Geochem., 21(12), 2188–2200.
Abstract: Phosphate-induced metal stabilization involving the reactive medium Apatite II(TM) [Ca10-xNax(PO4)6-x(CO3)x(OH)2], where x < 1, was used in a subsurface permeable reactive barrier (PRB) to treat acid mine drainage in a shallow alluvial groundwater containing elevated concentrations of Zn, Pb, Cd, Cu, SO4 and NO3. The groundwater is treated in situ before it enters the East Fork of Ninemile Creek, a tributary to the Coeur d'Alene River, Idaho. Microbially mediated SO4 reduction and the subsequent precipitation of sphalerite [ZnS] is the primary mechanism occurring for immobilization of Zn and Cd. Precipitation of pyromorphite [Pb10(PO4)6(OH,Cl)2] is the most likely mechanism for immobilization of Pb. Precipitation is occurring directly on the original Apatite II. The emplaced PRB has been operating successfully since January of 2001, and has reduced the concentrations of Cd and Pb to below detection (2 μg L-1), has reduced Zn to near background in this region (about 100 μg L-1), and has reduced SO4 by between 100 and 200 mg L-1 and NO3 to below detection (50 μg L-1). The PRB, filled with 90 tonnes of Apatite II, has removed about 4550 kg of Zn, 91 kg of Pb and 45 kg of Cd, but 90% of the immobilization is occurring in the first 20% of the barrier, wherein the reactive media now contain up to 25 wt% Zn. Field observations indicate that about 30% of the Apatite II material is spent (consumed).
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Heal, K. V., & Salt, C. A. (1999). Treatment of acidic metal-rich drainage from reclaimed ironstone mine spoil. Water Sci. Technol., 39(12), 141–148.
Abstract: Ironstone mine spoil leaves a legacy of land contamination and diffuse water pollution with acidic, metal-rich drainage. Reclamation for woodland may exacerbate water pollution due to spoil amendment and disturbance. Constructed wetland systems (CWS) are increasingly used for treating acid mine drainage but their performance is poorly understood. A combined approach was used to reclaim the Benhar ironstone spoil heap in Central Scotland. Trees have been planted in spoil treated with dried pelleted sewage sludge, limestone and peat. Spoil drainage (pH 2.7, 247 mg l-1 total Fe) passes through a CWS. Spoil throughflow, surface water chemistry and CWS performance were monitored for 12 months after reclamation. Acidity, Fe, Mn and Al concentrations declined in throughflow after reclamation, although this effect was not uniform. Soluble reactive P has been mobilised from the sewage sludge in residual areas of spoil acidity, but losses of other nutrients were short-lived. The CWS removes on average 33 % and 20-40 % of acidity and metal inputs but removal rates decrease in winter. Spoil reclamation has been successful in enabling vegetation establishment but has also increased Fe and Mn concentrations in surface drainage from the site, even after passage through the CWS.
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Blowes, D. W., Ptacek, C. J., Benner, S. G., McRae, C. W. T., Bennett, T. A., & Puls, R. W. (2000). Treatment of inorganic contaminants using permeable reactive barriers. J Contam Hydrol, 45(1-2), 123–137.
Abstract: Permeable reactive barriers are an emerging alternative to traditional pump and treat systems for groundwater remediation. This technique has progressed rapidly over the past decade from laboratory bench-scale studies to full-scale implementation. Laboratory studies indicate the potential for treatment of a large number of inorganic contaminants, including As, Cd, Cr, Cu, Hg, Fe, Mn, Mo, Ni, Pb, Se, Tc, U, V, NO3, PO4 and SO4. Small-scale field studies have demonstrated treatment of Cd, Cr, Cu, Fe, Ni, Pb, NO3, PO4 and SO4. Permeable reactive barriers composed of zero-valent iron have been used in full-scale installations for the treatment of Cr, U, and Tc. Solid-phase organic carbon in the form of municipal compost has been used to remove dissolved constituents associated with acid-mine drainage, including SO4, Fe, Ni, Co and Zn. Dissolved nutrients, including NO3 and PO4, have been removed from domestic septic-system effluent and agricultural drainage.
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Johnson, D. B., & Hallberg, K. B. (2005). Acid mine drainage remediation options: a review. Science of the Total Environment, 338(1-2), 3–14.
Abstract: Acid mine drainage (AMD) causes environmental pollution that affects many countries having historic or current mining industries. Preventing the formation or the migration of AMD from its source is generally considered to be the preferable option, although this is not feasible in many locations, and in such cases, it is necessary to collect, treat, and discharge mine water. There are various options available for remediating AMD, which may be divided into those that use either chemical or biological mechanisms to neutralise AMD and remove metals from solution. Both abiotic and biological systems include those that are classed as “active” (i.e., require continuous inputs of resources to sustain the process) or “passive” (i.e., require relatively little resource input once in operation). This review describes the current abiotic and bioremediative strategies that are currently used to mitigate AMD and compares the strengths and weaknesses of each. New and emerging technologies are also described. In addition, the factors that currently influence the selection of a remediation system, and how these criteria may change in the future, are discussed.
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Matlock, M. M., Howerton, B. S., & Atwood, D. A. (2002). Chemical precipitation of heavy metals from acid mine drainage. Water Res, 36(19), 4757–4764.
Abstract: The 1,3-benzenediamidoethanethiol dianion (BDET, known commercially as MetX) has been developed to selectively and irreversibly bind soft heavy metals from aqueous solution. In the present study BDET was found to remove >90% of several toxic or problematic metals from AMD samples taken from an abandoned mine in Pikeville, Kentucky. The concentrations of metals such as iron, may be reduced at pH 4.5 from 194 ppm to below 0.009 ppm. The formation of stoichiomietric BDET-metal precipitates in this process was confirmed using X-ray powder diffraction (XRD), proton nuclear magnetic resonance (1H NMR), and infrared spectroscopy (IR).
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