• Journal of Soil and Groundwater Environment
• /
• v.27 no.4
• /
• pp.10-21
• /
• 2022

In the South Korea, 47% of abandoned mines are suffering from the mining hazards such as the mine drainage (MD), the mine tailings and the waste rocks. Among them the mine drainage which has a low pH and the high concentration of heavy metals can directly contaminate rivers or soil and cause serious damages to human health. The natural/artificial treatment facilities by using neutralizers and coagulants for the mine drainage have been operated in domestic and most of heavy metals in mind drainage are precipitated and removed in the form of metal hydroxide, alumino-silicate or carbonate, generating a large amount of mine drainage treated sludge ('MDS' hereafter) by-product. The MDS has a large surface area and many functional groups, showing high efficiency on the fixation of heavy metals. The purpose of this study is to develop a ingenious heavy metal stabilizer that can effectively stabilize arsenic (As) and heavy metals in soil by recycling the MDS (two types of MDS: the acid mine drainage treated sludge (MMDS) and the coal mine drainage treated sludge (CMDS)). Various analyses, toxicity evaluations, and leaching reduction batch experiments were performed to identify the characteristics of MDS as the stabilizer for soils contaminated with As and heavy metals. As a result of batch experiments, the Pb stabilization efficiency of both of MDSs for soil A was higher than 90% and their Zn stabilization efficiencies were higher than 70%. In the case of soil B and C, which were contaminated with As, their As stabilization efficiencies were higher than 80%. Experimental results suggested that both of MDSs could be successfully applied for the As and heavy metal contaminated soil as the soil stabilizer, because of their low unit price and high stabilization efficiency for As and hevry metals.

• Economic and Environmental Geology
• /
• v.37 no.1
• /
• pp.107-111
• /
• 2004

This study was undertaken to summarize of the efficiencies of the passive treatment system and suggest future studies for the solution of mine drainage problem. Flow rates of mine drainage from the abandoned coal mines are about 80,000 ton/day. Contaminated mine drainages over about 50 ton/day of flow rate were treated by passive treatment facilities such as Successive Alkalinity Producing Systems(SAPS), oxidation pond and oxic wetland. Chemical analysis for 13 passive coal mine treatment facilities showed that SAPS was the core of treatment facilities because the variation of Fe removal rates was relatively smaller than any other processes and re-leaching of Fe was not measured. The performance and life of SAPS depended on decrease in permeability and retention time due to accumulation of sludge. It is inferred that upgrade of design of the passive treatment system and in-situ treatment using underground void will be necessary for the amelioration of the mine drainage with high metal loading rates.

• Applied Chemistry for Engineering
• /
• v.16 no.3
• /
• pp.391-396
• /
• 2005

This study was conducted to neutralize acid mine drainage (AMD) of Soo and Hambaek mines, located in Kangwon-Do Korea, using $Ca(OH)_2$. When 0.295 g $Ca(OH)_2/L$(AMD) was added to the drainage in a neutralization reactor, pH of liquid in the reactor and the effluent were maintained at 9.5 and 8.4, respectively. The pH met the required effluent standard. With 10~50% of feedback of effulent sludge to the reactor, the pH of neutralized fluid in the reactor remained nearly constant, but $SO{_4}^{-2}$ concentration in the effluent increased adversely compared to the non-return sludge case. With 30% of sludge feedback, it was possible to decrease suspended solids (SS) concentration in the effluent without a problem in Fe concentration. When 100 mL of 0.1 M $BaCl_2$ was added to 1 L of AMD treated with $Ca(OH)_2$, removal efficiency of $SO{_4}^{-2}$ increased to over 90%. Aanalyses of pH, Fe, and $SO{_4}^{-2}$ showed that the optimal results were obtained when pH of neutralizatio reactor and sludge return ratio were maintained at 9.5 and 30%. This can result in possible cost reduction of 31.4% for maintenance and 29.8% for facility construction by alternating $Ca(OH)_2$ to NaOH.

• Journal of Korea Soil Environment Society
• /
• v.2 no.1
• /
• pp.45-50
• /
• 1997

The change of industrial structure has brought the sharp declination of mine products, and has made many mines closed, which results in environmental pollution by untreated acid mine drainage(AMD). AMD with low pH and high concentration of heavy metals could severely destroy the ecosystem. Many researches have been carried out for the treatment of AMD. In this study, we have treated AMD with oak compost, mushroom compost, sludge cake and cow manure which usually used in AMD treatment systems, and compared the capability of each organic matter. Cow manure and oak compost have been most effective among 4 organic materials. Oak compost removed the heavy metals by ion exchange between Ca-rich particles and soluble heavy metal ions. It also captured the heavy metals using bound functional groups like -OH and -COO-. Sulfate reducing bacteria existing in the cow manure removed effectively heavy metals by producing metal sulfide compound. Therefore, it is effective to use both organic materials in mixture on the treatment of AMD.

• Economic and Environmental Geology
• /
• v.56 no.2
• /
• pp.125-138
• /
• 2023

Most of previous cesium (Cs) sorbents have limitations on the treatment in the large-scale water system having low Cs concentration and high ion strength. In this study, the new Cs sorbent that is eco-friendly and has a high Cs removal efficiency was developed by improving the coal mine drainage treated sludge (hereafter 'CMDS') with the addition of Na and S. The sludge produced through the treatment process for the mine drainage originating from the abandoned coal mine was used as the primary material for developing the new Cs sorbent because of its high Ca and Fe contents. The CMDS was improved by adding Na and S during the heat treatment process (hereafter 'Na-S-CMDS' for the developed sorbent in this study). Laboratory experiments and the sorption model studies were performed to evaluate the Cs sorption capacity and to understand the Cs sorption mechanisms of the Na-S-CMDS. The physicochemical and mineralogical properties of the Na-S-CMDS were also investigated through various analyses, such as XRF, XRD, SEM/EDS, XPS, etc. From results of batch sorption experiments, the Na-S-CMDS showed the fast sorption rate (in equilibrium within few hours) and the very high Cs removal efficiency (> 90.0%) even at the low Cs concentration in solution (< 0.5 mg/L). The experimental results were well fitted to the Langmuir isotherm model, suggesting the mostly monolayer coverage sorption of the Cs on the Na-S-CMDS. The Cs sorption kinetic model studies supported that the Cs sorption tendency of the Na-S-CMDS was similar to the pseudo-second-order model curve and more complicated chemical sorption process could occur rather than the simple physical adsorption. Results of XRF and XRD analyses for the Na-S-CMDS after the Cs sorption showed that the Na content clearly decreased in the Na-S-CMDS and the erdite (NaFeS₂·2(H₂O)) was disappeared, suggesting that the active ion exchange between Na⁺ and Cs⁺ occurred on the Na-S-CMDS during the Cs sorption process. From results of the XPS analysis, the strong interaction between Cs and S in Na-S-CMDS was investigated and the high Cs sorption capacity was resulted from the binding between Cs and S (or S-complex). Results from this study supported that the Na-S-CMDS has an outstanding potential to remove the Cs from radioactive contaminated water systems such as seawater and groundwater, which have high ion strength but low Cs concentration.