• Journal of the Korea Academia-Industrial cooperation Society
• /
• v.7 no.3
• /
• pp.453-457
• /
• 2006

A long-term leaching column experiment was performed to evaluate the teachability of the stabilized lead-contaminated soil using soluble phosphate. The study shows that Pb in the leachate was little detected and the remaining $PO_4-P$ concentration kept below 0.1 mg/L due to the formation of geochemically stable lead phosphate minerals from the reactions of labile soil Pb forms with the added soluble phosphate salt. After the experiment, there was no Pb migration from the top to the bottom of the stabilized soil column. But the Pb concentrations of the 12 soil samples from the control column decreased with the increase of the soil depth.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
• /
• 2000.11a
• /
• pp.252-257
• /
• 2000

연구 결과를 간단히 요약하면 다음과 같다. 1) 온천 목적으로 개발된 국내 심부 암반 지하수(조사 대상 시료수 419개)는 화강암 및 화강편마암 지역에서 가장 높은 불소 함량을 보이며, 최소 75% 이상의 시료에서 먹는 물 수질 기준을 초과하였다. 2) 화강암 및 화강편마암 지역의 심부 지하수 내 불소 함량은 특히 Na-HCO$_3$ 유형의 지하수에서 높게 나타났는데, 이 유형의 지하수 수질은 사장석, 흑운모를 위시한 규산염 광물의 비조화 용해 반응에 의해 조절된다 이들 지하수는 비교적 깊은 관정심도를 나타내었다. 3) 백악기 화강암과 물과의 용출 반응 실험 결과, 전암 분말과의 반응에서는 최대 7 mg/l의 불소가, 흑운모의 용출 실험에서는 최대 35 mg/1의 불소가 용출되었다. 형석의 포화지수는 비교적 반응 초기에 침전 조건에 근접한 반면, 흑운모의 포화지수는 지속적으로 용해 조건에 놓여 있음을 확인하였다. 따라서, 국내 화강암 지역 심부 지하수 내의 불소는 대부분 흑운모의 비조화 용해 반응에 의해 용출되며, 용출 이후에는 형석의 용해/침전 평형 반응에 의해 그 농도가 조절되는 것으로 확인된다. 4) 앞으로, 보다 자세한 평형 열역학적 해석과 다른 이온종과의 상호 관계 규명 및 광물학적 검토를 통하여 불소의 기원과 거동에 관한 보다 정확한 해석을 시도할 계획이다.

• Korean Journal of Mineralogy and Petrology
• /
• v.33 no.3
• /
• pp.243-250
• /
• 2020

The purpose of this study is to find out the possibility of applying microwave-hypochlorous acid leaching to effectively leaching Au in hydrothermal minerals on board. The comparative leaching experiment were confirmed that the leaching rate of Au with(T1)/with out(T2) of microwave nitric acid leaching. In addition, the leaching rate of Au on the conventional leaching by mechanical agitation(T3) and microwave leaching was compared. The result of microwave nitric acid leaching(solid-liquid ratio; 10%, leaching temperature; 90 ℃, leaching time; 20 min) confined that the metal leaching rate was high in the order of As>Pb>Cu>Fe>Zn, and the content of Au in the leaching residue was increased from 33.77 g/ton to 60.02 g/ton. As a result of the comparative leaching experiment using a chloride solvent, the dissolution rate of Au was high in the order of T1(61.10%)>T3(53.30%)>T2(17.30%). Therefore, chloride, which can be manufactured using seawater and that can be recycled by collecting chlorine gas generated in the leaching process, is expected to be an optimal solvent for Au leaching. In addition, the application of microwaves is believed to be effective in terms of time, efficiency and energy.

• Journal of Environmental Impact Assessment
• /
• v.26 no.3
• /
• pp.207-216
• /
• 2017

Several bioassays have been performed for assessment of the impact of polluted sediments. The direct exposure method using sediments is limited by difficulty controlling feeding and its effects on organisms. Furthermore, only macro-organisms and benthic organisms are used. To evaluate the potential application of sediment elutriate as a complementary strategy for impact assessment, copepods, small organisms with a short life cycle, were exposed to sediment elutriates, and several end-points were measured. As a result, sediment elutriates prepared from polluted sites caused growth retardation in marine copepods. In terms of molecular biomarkers, antioxidant-related and chaperone protein gene expression levels were increased in a dose- and time-dependent manner. Thus, we suggest that sediment elutriate tests can provide an effective alternative for toxicity assessment using whole sediment samples. Further studies are required to obtain sufficient data for future applications.

• Journal of Soil and Groundwater Environment
• /
• v.8 no.2
• /
• pp.62-69
• /
• 2003

The aim of research is the evaluation of the $Cr^{6+}$ emission features of the liquid injection through emission experiments in varying conditions, based on a field-mixing ratio. The results showed that the content of $Cr^{6+}$ content in cement measured had an Ordinary Potland Cement (OPC) of 25.3 mg/kg, which constitute the largest portion among the other materials. Likewise, the emission experiment of homo-gel and sand-gel generally satisfied the standard of KSLT (Korea Standard Leaching Test) in waste of 1.5 mg/L, but in case of the standard of KSLT in soil the emission of OPC $Cr^{6+}$ of 4.85 mg/kg. These conditions is a little exceeded the criteria in the ‘Ga’ area in terms of Korea Soil Environmental Preservation Law. In addition, results generated by the mock-up injection facilities revealed that $Cr^{6+}$ emission increased as Water/Cement and injection pressure increased. At injection pressure higher than 4 kg/㎤, $Cr^{6+}$ emission exceeded the water preservation standard of 0.5 mg/L. Similarly, a pattern experiment of C $r^{6+}$ emission according to pH was conducted, in order to evaluate the $Cr^{6+}$ emission features of grout materials in leachate below pH 5 such as pH 4 acid rain or landfill. Results show that $Cr^{6+}$ emission dramatically increased in high acidic or basic state. It indicates that $Cr^{6+}$ emission will probably increase in an environment where grout materials are injected. On the other hand, concentration of leachate was determined in areas where grout materials are used. The results show that the concentration of emission in an ultra purity condition does not manifest intensity, and is affected in the OPC>MC>SC order. It means that the pollutants or $Cr^{6+}$ emission increases with decreasing concentration. As such, $Cr^{6+}$ emission will probably exceed the countermeasure criteria according to the types of gout materials. Similarly, high pressure or injection will cause increased $Cr^{6+}$ emission. Therefore, the selection of materials or mixing ratio should be considered in general as well as according to specific industries, based on the strength and pH of $Cr^{6+}$ emission.

• Journal of Korea Soil Environment Society
• /
• v.2 no.2
• /
• pp.73-79
• /
• 1997

Removal of the Arsenic components from the closed mine tailings has been attempted by the alkali-leaching method. Two tailings collected from the Daduck and Yuchon mine which were already closed many years ago were leached with caustic soda solutions. The Arsenic components in the leach liquor resulted from the alkali treatment of tailings could be removed fairly well in the form of insoluble calcium-Arsenic compound by the precipitation with calcium chloride. As a result, the extraction of about 60~90% Arsenic from the tailings could be obtained depending on the leaching conditions and the influence of temperature and the slurry density on the extraction of Arsenic was also found to be very small at the NaOH concentration more than 0.5N. In addition, it seemed that a caustic soda solution over 0.5N NaOH could be used repeatedly for the leaching of tailings since the consumption of NaOH was not so great in a leaching of them. As far as the precipitation of Arsenic components was concerned, more than 99% of Arsenic could be precipitated within 10 minutes by the addition of 2wt% CaC12 in to the leach liquor.

• Journal of the Korean earth science society
• /
• v.29 no.3
• /
• pp.246-254
• /
• 2008

This study has been performed to evaluate the possibility of utilizing feldspar porphyry as an adsorbent for heavy metals in natural water. The research sample rock 'Maekbansuk' was altered feldspar porphyry which included chlorite, epidote and calcite formed by a prophylitic alteration process. In extraction tests, the majority of extracted elements were Ca and Na, which were extracted in much greater abundance from the groundmass than from the feldspar phenocryst. In adsorption tests, the adsorption capacities of Pb, Fe and Cu within an hour of reaction time were 99, 98 and 97%, respectively, but that of As remained 25% for a full 24 hours. The high adsorption capacities of altered feldspar porphyry for Pb, Fe and Cu suggest its potential utilization as a heavy metal adsorbent fur water purification.

• Resources Recycling
• /
• v.17 no.5
• /
• pp.44-51
• /
• 2008

The removal of minor elements such as Na, Ca and Fe has been performed from domestic aluminum hydroxide of 99.7% purity with organic acids. Oxalic and citric acid were used as the leaching agent, respectively and aluminum hydroxides of different particle size were also employed for the purification with organic acid leaching. Fine grinding of aluminum hydroxide has been tested using ball mills and leaching characteristics of each element have also been examined in terms of leaching parameters such as temperature, acid concentration, and solid density. As a result, it was found that oxalic acid showed higher leaching efficiency than citric acid in the concentration range of 0.1 to 1.0 mole/l and leaching amount of each element was also increased with the acid concentration and reaction temperature. It was observed that about 45% of Na was leached out during ball milling process which implied that the majority of Na contained in aluminum hydroxide was water soluble compound.

• Analytical Science and Technology
• /
• v.15 no.1
• /
• pp.72-79
• /
• 2002

Di-(2-ethylhexyl)phthalate (DEHP) may be released from plasticized poly(vinyl chloride) (PVC) articles. In the cases of various methods for the quantitative analysis of migrating DEHP, there are much differences in migrating quantity according to the experimental methods. It is therefore important to make the comparison and analysis between these two results. A study of DEHP migration from blood and infusion bags has been carried out in different methods to evaluate the amount of DEHP migration using gas chromatograph and UV-vis spectrophotometry. Five PVC bags were cut into plane sheets in size of $40{\times}10{\times}0.4mm$, then were immersed in extraction solvent for an hour to release DEHP. It was determined by a gas chromatograph that $23.2{\sim}70.9{\mu}g/mL$ of DEHP was extracted. While extraction solvent was injected into PVC bags which were then placed for an hour to leach DEHP out. It was checked by a UV-vis spectrophotometer that the concentration of DEHP in extraction solvent was $24.8{\sim}41.3{\mu}g/mL$. Two results show different values according to the extraction conditions and experimental methods and the gas chromatographic results were converted into UV-vis spectroscopic results on condition that DEHP would be extracted equally per unit time and unit contact area. It was concluded that DEHP migrating amounts are approximately equal in two analytical methods.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
• /
• 2005.04a
• /
• pp.9-12
• /
• 2005

각기 다른 경로로 카드뮴에 오염된 두 토양에서 카드뮴을 중성인 물과 황산 수용액으로 용출하여 보았다. 토양은 자연에서 오랫동안 오염된 금속 폐 광산 토양과 한편으로는 오염되지 않은 토양을 인공적으로 오염시킨 것 두 가지를 재료로 사용하였다. 실험결과, 높은 카드뮴 농도에도 불구하고 자연오염 토양의 경우 추출용매가 물인 경우에는 카드뮴이 거의 용출되지 않았고 산 용액에서는 상대적으로 낮은 농도의 카드뮴이 꾸준히 용출되었다. 이에 반하여 인공오염토양의 경우 카드뮴의 용출량이 많아, 현실적으로 공장부지 등지에서 급격히 오염된 토양에는 산성비가 내릴 경우 카드뮴이 지하수를 오염시킬 위험성이 금속 폐광산등 자연적으로 오염된 토양에서보다 상대적으로 더 큰 것으로 나타났다. 특히 중성인 물에서도 인공오염토양 내 카드뮴의 초기 용출량이 크게 나타났는데, 이것은 공단부지 등에서 상대적으로 토양의 카드뮴 오염이 빠르게 진행된 지역의 지하수 등이 카드뮴 오염에 상대적으로 크게 노출되어 있음을 의미한다.