Natural attenuation of arsenic in the wetland system around abandoned mining area

Mechanisms of natural attenuation of arsenic (As) by wetland plants may be classified by plant uptake and adsorption and/or co-precipitation by iron (oxy)hydroxide formed on the root surface of plants or in rhizosediment. A natural Cattail (Typha spp.) wetland impacted by tailings containing high levels of As from the Myungbong abandoned Au Mine, South Korea was selected, and the practical capability of this wetland to attenuate As was evaluated. The As concentrations in the plant tissues from the study wetland were several-fold higher than those from control wetland. SEM-EDX analyses demonstrated that iron plaques exist on the rhizome surface. Moreover, relatively high As contents bonded with hydrous iron oxides were found in the rhizosediments rather than in the bulk sediments. It was revealed through the leaching and sequential extraction analyses that As existed as more stable forms in the wetland sediment compared with adjacent paddy soil, which is also contaminated with As due to input of mine tailings. The As concentration ratios of extracted solution to sediment/soil represented that the wetland sediment showed significant lower values (10-fold) rather than the paddy soil with indicating high As stability. Also, As in the wetland sediment was predominantly bonded with residual phases on the basis of results from sequential extraction analysis. From these results, it is concluded that transformation of As contaminated agricultural field to wetland environment may be helpful for natural attenuation until active remediation action.     

Potential application of sludge produced from coal mine drainage treatment for removing Zn(II) in an aqueous phase

Various analyses of physico-chemical characteristics and batch tests were conducted with the sludge obtained from a full-scale electrolysis facility for treating coal mine drainage in order to find the applicability of sludge as a material for removing Zn(II) in an aqueous phase. The physico-chemical analysis results indicated that coal mine drainage sludge (CMDS) had a high specific surface area and also satisfied the standard of toxicity characteristic leaching procedure (TCLP) because the extracted concentrations of certain toxic elements such as Pb, Cu, As, Hg, Zn, and Ni were much less than their regulatory limits. The results of X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) showed that the CMDS mainly consists of goethite (70%) and calcite (30%) as a weight basis. However, the zeta potential analysis represented that the CMDS had a lower isoelectric point of pH (pH_IEP) than that of goethite or calcite. This might have been caused by the complexation of negatively charged anions, especially sulfate, which usually exists with a high concentration in coal mine drainage. The results of Fourier transform infrared (FT-IR) spectrometry analysis revealed that Zn(II) was dominantly removed as a form of precipitation by calcite, such as smithsonite [ZnCO₃] or hydrozincite [Zn₅(CO₃)₂(OH)₆]. Recycling sludge, originally a waste material, for the removal process of Zn(II), as well as other heavy metals, could be beneficial due to its high and speedy removal capability and low economic costs.     

Application of powdered activated carbon coating to fabrics in a hybrid filter to enhance mercury removal

Elemental mercury(Hg0) is predominant constituent of flue gas emitted from coal-fired power plants. Adsorption has been considered the best available technology for removal of Hg0 from flue gas. However, adsorbent injection increases the amount of ash generated. In the present study, powdered activated carbon(PAC) was coated on polytetrafluoroethylene/glass fiber filters to increase Hg0 removal while concurrently reducing the amount of ash generated. The optimal PAC coating rate was determined in laboratory experiments to ensure better Hg0 removal with low pressure drop. When PAC of particle size less than 45 μm was used, and the areal density was 50 g/m2, the pressure drop remained under 30 Pa while the Hg0 removal efficiency increased to 15.8% from4.3%. The Hg0 removal efficiency also increased with decrease in filtration velocity. The optimal PAC coating rate was applied on a hybrid filter(HF), which was combined with a bag filter and an electrostatic precipitator in a single chamber. Originally designed to remove fine particulates matter, it was retrofitted to the flue gas control device for simultaneous Hg0 removal. By employing the PAC coating, the Hg removal efficiency of the HF increased to 79.79% from 66.35%. Also, a temporary reduction in Hg removal was seen but this was resolved following a cleaning cycle in which the dust layer was removed.     

Effect of preparation method of noble metal supported catalyts on formaldehyde oxidation at room temperature: Gas or liquid phase reduction

Formaldehyde (HCHO) is toxic to the human body and is one of the main threats to the indoor air quality (IAQ). As such, the removal of HCHO is imperative to improving the IAQ, whereby the most useful method to effectively remove HCHO at room temperature is catalytic oxidation. This review discusses catalysts for HCHO room-temperature oxidation, which are categorized according to their preparation methods, i.e., gas-phase reduction and liquid-phase reduction methods. The HCHO oxidation performances, structural features, and reaction mechanisms of the different catalysts are discussed, and directions for future research on catalytic oxidation are reviewed.     

Regional assessment of groundwater quality for drinking purpose

Owing to limited surface water during a long-term drought, this work attempted to locate clean and safe groundwater in the Choushui River alluvial fan of Taiwan based on drinking-water quality standards. Because aquifers contained several pollutants, multivariate indicator kriging (MVIK) was adopted to integrate the multiple pollutants in groundwater based on drinking- and raw-water quality standards and to explore spatial uncertainty. According to probabilities estimated by MVIK, safe zones were determined under four treatment conditions—no treatment; ammonium–N and iron removal; manganese and arsenic removal; and ammonium–N, iron, manganese, and arsenic removal. The analyzed results reveal that groundwater in the study area is not appropriate for drinking use without any treatments because of high ammonium–N, iron, manganese, and/or arsenic concentrations. After ammonium–N, iron, manganese, and arsenic removed, about 81.9–94.9% of total areas can extract safe groundwater for drinking. The proximal-fan, central mid-fan, southern mid-fan, and northern regions are the excellent locations to pump safe groundwater for drinking after treatment. Deep aquifers of exceeding 200 m depth have wider regions to obtain excellent groundwater than shallow aquifers do.     

Use of multivariate indicator kriging methods for assessing groundwater contamination extents for irrigation

Multivariate geostatistical approaches have been applied extensively in characterizing risks and uncertainty of pollutant concentrations exceeding anthropogenic regulatory limits. Spatially delineating an extent of contamination potential is considerably critical for regional groundwater resources protection and utilization. This study used multivariate indicator kriging (MVIK) to determine spatial patterns of contamination extents in groundwater for irrigation and made a predicted comparison between two types of MVIK, including MVIK of multiplying indicator variables (MVIK-M) and of averaging indicator variables (MVIK-A). A cross-validation procedure was adopted to examine the performance of predicted errors, and various probability thresholds used to calculate ratios of declared pollution area to total area were explored for the two MVIK methods. The assessed results reveal that the northern and central aquifers have excellent groundwater quality for irrigation use. Results obtained through a cross-validation procedure indicate that MVIK-M is more robust than MVIK-A. Furthermore, a low ratio of declared pollution area to total area in MVIK-A may result in an unrealistic and unreliable probability used to determine extents of pollutants. Therefore, this study suggests using MVIK-M to probabilistically determine extents of pollutants in groundwater.     

Application of portable X-ray fluorescence (pXRF) for heavy metal analysis of soils in crop fields near abandoned mine sites

To get representative soil samples, a sampling method was verified for crop fields in the vicinity of abandoned mine sites. Application of appropriate sampling or analytical methods is very important as it affects the costs, time, and accuracy of the refined investigation of soil contamination. Two-time sampling for each crop field was conducted to verify the reproducibility of a zigzag method for soil sampling. The soil analysis using a portable X-ray fluorescence (pXRF) device was conducted to measure concentrations of metal species in soils, and its results were compared to the extracted concentrations by the Korean Standard Test (KST) for soils. As a result, the determination coefficient (R ²) of linear regression analysis for data obtained by ex situ precise measurement or in situ field screening using pXRF was closely related with the ratio of the extracted concentration by KST to interference-free detection limits (IFDL) of pXRF (designated as KST/IFDL). As the specific metal species had a higher ratio of KST/IFDL, its R ² was even higher in the field screening tests. However, the slopes of linear regression analysis for most metal species extracted by aqua-regia were close to 1.0 so that extracted concentrations by aqua-regia were similar to the analytical values obtained by pXRF, whereas extraction using a weak acid (0.1 M HCl) had different slopes for soils contaminated with different ranges of concentrations of metal species. Especially Zn showed not only high ratios of KST/IFDL because of aqua regia extraction, but also high determination coefficients. Because of its simple, rapid, and accurate capacities for metal analysis, the pXRF analysis showed high applicability in ex situ precise measurements or in situ field screening of metal analysis. In terms of applicability for regulation, especially in situ pXRF field screening with the zigzag method could be effectively applied to achieve an economical survey by determining hot spots or non-contaminated areas if aqua-regia was applied as the extracting agent in the KST for soils.     

Assessment of Young Dong tributary and Imgok Creek impacted by Young Dong coal mine, South Korea

An initial reclamation of the Young Dong coal mine site, located in northeastern South Korea, was completed in 1995. Despite the filling of the adit with limestone, acid rock drainage (ARD) enters Young Dong tributary and is then discharged to Imgok Creek. This ARD carries an average of 500 mg CaCO(3)/l of mineral acidity, primarily as Fe(II) and Al. Before spring runoff, the flow of Imgok Creek is 3.3-4 times greater than that of the tributary and has an alkalinity of 100 mg CaCO(3)/l, which is sufficient to eliminate the mineral acidity and raise the pH to about 6.5. From April through September 2008, there were at least two periods of high surface flow that affects the flow of ARD from the adit. Flow of ARD reaches 2.8 m(3)/min during spring runoff. This raised the concentrations of Fe and Al in the confluence with Imgok Creek. However, by 2 km downstream the pH of the Imgok Creek is 6.5 and only dissolved Fe is above the Korean drinking water criteria (0.30 mg/l). This suggests only a minor impact of Young Dong Creek water on Imgok Creek. Acid digestion of the sediments in Imgok Creek and Young Dong Tributary reveals considerable abundances of heavy metals, which could have a long-term impact on water quality. However, several water-based leaching tests, which better simulate the bioavailable metals pool, released only Al, Fe, Mn, and Zn at concentrations exceeding the criteria for drinking water or aquatic life.     

Long-term assessment of the environmental fate of heavy metals in agricultural soil after cessation of organic waste treatments

The current study examined the anthropogenic accumulation and natural decrease in metal concentrations in agricultural soils following organic waste application. Three common organic wastes, including municipal sewage sludge, alcohol fermentation processing sludge, and pig manure compost (PMC), were applied annually to an agricultural soil under field conditions over 7 years (1994–2000) at a rate of 12.5, 25, and 50 ton ha^?1 year^?1 and the soil accumulation of three metals of concern (Cu, Pb, and Zn) was monitored. Subsequently, organic waste amendments ceased and the experimental plots were managed using conventional fertilization for another 10 years (2001–2010) and the natural decrease in metal concentrations monitored. Although Cu and Zn concentrations in all experimental plots did not exceed the relevant guideline values (150 mg kg^?1 for Cu and 300 mg kg^?1 for Zn), significant increases in metal concentrations were observed from cumulative application of organic wastes over 7 years. For instance, PMC treatment resulted in an increase in Cu and Zn from 9.8 and 72 mg kg^?1 to 108.2 and 214.3 mg kg^?1, respectively. In addition, the natural decrease in Cu and Zn was not significant as soils amended with PMC showed only a 16 and 19 % decline in Cu and Zn concentrations, respectively, even 10 years after amendment ceased. This research suggested that more attention must be paid during production of organic waste-based amendments and at the application stage.     

End-of-life batteries management and material flow analysis in South Korea

Analysis of collection and recycling system of end-of-life batteries was examined. Relatively limited fractions of portable batteries were collected by EPR system. More effective and diverse collection pathways should be developed. Consumers increasingly have worn-out batteries as electrical and electronic equipment with new technical developments are introduced into the market and quickly replace older models. As a result, large amounts of end-of-life (EOL) or waste batteries are generated. Such batteries may contain a variety of materials that includes valuable resources as well as toxic elements. Thus, the proper recycling and management of batteries is very important from the perspective of resource conservation and environmental effect. The collection and recycling of EOL batteries is relatively low in South Korea compared to other countries, although an extended producer responsibility (EPR) policy was adopted for battery recycling in 2003. In this study, the management and material flow of EOL batteries is presented to determine potential problems and quantitative flow, based on literature review, site visits to battery recycling facilities, and interviews with experts in the Korea Battery Recycling Association (KBRA), manufacturers, and regulators in government. The results show that approximately 558 tons of manganese-alkaline batteries, the largest fraction among recycling target items, was disposed in landfills or incinerators in 2015, while approximately 2,000 tons of batteries were recovered at a recycling facility by simple sorting and crushing processes. By raising environmental awareness, more diverse and effective collection systems could be established for consumers to easily dispose of EOL batteries in many places. Producers, retailers and distributors in South Korea should also play an important role in the collection of EOL batteries from consumers. Lithium-ion batteries from many electronic devices must be included in the EPR system for resource recovery.