|
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.
|
|
|
Sato, D., & Tazaki, K. (2000). Calcification treatment of mine drainage and depositional formula of heavy metals. Chikyu Kagaku = Earth Science, 54(5), 328–336.
Abstract: Depositional formula of heavy metals after disposal of the mine drainage from the Ogoya Mine in Ishikawa Prefecture, Japan, was mineralogically investigated. Strong acidic wastewater (pH 3.5) from pithead of the mine contains high concentration of heavy metals. In this mine, neutralizing coagulation treatment is going on by slaked lime (calcium hydroxides: Ca(OH) (sub 2) ). Core samples were collected at disposal pond to which the treated wastewater flows. The core samples were divided into 44 layers based on the color variation. The mineralogical and chemical compositions of each layer were analyzed by an X-ray powder diffractometer (XRD), an energy dispersive X-ray fluorescence analyzer (ED-XRF) and a NCS elemental analyzer. The upper parts are rich in brown colored layers, whereas discolored are the deeper parts. The color variation is relevant to Fe concentration. Brown colored core sections are composed of abundant hydrous ferric oxides with heavy metals, such as Cu, Zn, and Cd. On the other hand, S concentration gradually increases with depth. XRD data indicated that calcite decreases with increasing depth, and ettringite is produced at the deeper parts. Cd concentration shows similar vertical profile to those of calcite and ettringite. The results revealed that hydrous ferric oxides, calcite and ettringite are formed on deposition, whereby incorporating the heavy metals.
|
|
|
Dillard, G. (2000). A win-win way to clean up by changing ionic state, new process can precipitate heavy metals. Pay Dirt, 734, 10–11.
|
|
|
Willscher, S. (2001). Loesungsansaetze zur Minderung der Umweltbelastung durch saure Grubenwaesser; I, Massnahmen zu deren Minimierung und Verfahren der aktiven Behandlung. Approaches for reducing environmental pollution by acid mine drainage; I, Mitigation measures and methods for active remediation. Vom Wasser, 97, 145–166.
|
|
|
Sottnik, P., & Sucha, V. (2001). Moznosti upravy kysleho banskeho vytoku loziska Banska Stiavnica-Sobov. Remediation of acid mine drainage from Sobov Mine, Banska Stiavnica. Mineralia Slovaca, 33(1), 53–60.
Abstract: A waste dump formed during the exploitation of quartzite deposit in Sobov mine (Slovakia) produces large quantity of acid mine drainage (AMD) which is mainly a product of pyrite oxidation. Sulphuric acid--the most aggressive oxidation product--attacks gangue minerals, mainly clays, as well. This process lead to a sharp decrease of the pH values (2-2.5) and increase of Fe, Al and SO (super 2-) (sub 4) contents (TDS = 20-30 mg/1). Passive treatment system was designed to remediate AMD. Chemical redox reactions along with microbial activity cause a precipitation of mobile contamination into a more stable forms. The sulphides are formed in the anaerobic cell, under reducing conditions. Fe-, Al- oxyhydroxides are precipitated in the aerobic part of the system. Precipitation decreases the Fe and Al contents along with immobilization of some heavy metal closely related to oxyhydroxides. Besides oxidation, the wetland vegetation is an active part of on aerobic cell. The system has been working effectively since September 1999. The pH values of outflowing water are apparently higher (6.2-6.8) and contents of dissolved elements (Fe from 2.260 to 4.1; Al from 900 to 0.18; Mn from 51 to 23; Cu from 4.95 to 0.03 mg/l) is significantly lowers.
|
|