• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2005.04a
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• pp.182-185
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• 2005

울산광산 내 지표수와 토양 중의 공극수에 함유되어 있는 비소의 오염현황을 파악하고, pH와 산화-환원 전위 값의 변화에 따른 자연저감 능력을 평가하였다. 유비철석을 비롯한 비소함유 광물은 높은 산화-환원 전위 값과 낮은 pH 조건에서 해리되며, 이후 지하수의 진화과정에서 pH가 상승함에 따라 주로 5가의 비소형태로 존재하게 된다. 울산광산지역 지하수의 비소농도는 Eh가 높은 비포화대와 포화대 지하수의 경계부에서 높은 경향을 나타내며, 포화대의 상부에서는 Eh가 비교적 일정하나 비소 농도는 다양한 분포양상을 보인다. 포화대 하부에서 비소의 함량은 매우 낮으며, Eh 감소에 따라 비소 함량이 비례적으로 감소한다. 반응경로 과정에서 비소농도는 Eh<-0.1(V)인 지하수 포화대에서 가장 낮으며, pH가 상대적으로 낮고 산화-환원 전위값이 높은 비포화대에서 증가되는 경향을 보인다. 풍화 반응 정도가 높은 광미와 토양에서 비소농도 높으나, 용출실험에서 비소가 기준치 이하로 용출되는 것은 풍화반응과 토양에 의한 비소의 자연저감이 진행되고 있음을 반영한다. RMB를 이용한 중금속 제거능력 평가 실내실험에서, 산성과 알칼리 조건 모두에서 제거율이 높은 것으로 나타났다. 인회석과 철산화물질로 구성된 RMB는 친환경적이고 2차 오염문제를 극복할 수 있는 물질로서, 비소의 자연저감 능력을 향상시킬 수 있는 정화처리제로 활용이 가능할 것으로 판단된다.

• Journal of Korean Society of Environmental Engineers
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• v.32 no.6
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• pp.631-638
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• 2010

The objective of this study was to evaluate the efficiency of zerovalent iron and basic oxygen furnace slag on arsenic stabilization in soils. For this, arsenic (V) contaminated soil and roxarsone contaminated soil were incubated after incorporation with zerovalent iron (ZVI) or basic oxygen furnace slage (BOFS) at four different levels (0%, 1%, 3%, and 5%) for 30 days and then the residual concentrations of arsenic were analysed following extraction with aqua reqia, 1N HCl and 0.01 M $CaCl_2$. The total concentration of arsenic was 2,285 mg/kg in the As(V) contaminated soil and 6.5 mg/kg in the roxarsone contaminated soil. 1 N HCl extractable arsenic concentration in the As(V) contaminated soil was initially 1,351 mg/kg and this was significantly declined by 713~1,034 mg/kg following incubation with ZVI while BOFS treatment showed no effect on the stabilization of inorganic arsenate except 5% treatment which showed around 100 mg/kg reduction in 1N HCl extractable arsenic. Similarly, in the roxarsone contaminated soil 1N HCl extractable concentration of arsenic was reduced from 3.13 mg/kg to 0.69 mg/kg with ZVI treatment increased from 1% to 5% while BOFS treatment did not lead to any statistically significant reduction. Available (0.01M $CaCl_2$ extractable) arsenic was initially 0.85 mg/kg in the As(V) contaminated soil and this declined by 0.79 mg/kg following incorporation with 5% ZVI, which accounted for more than 90% of the available As in the control. When As(V)-contaminated soil was treated with BOFS, the available arsenic was increased due to competing effect of the phosphate originated from BOFS with arsenate for the adsorption sites. For the roxarsone contaminated soil, the greater the treatment of ZVI or BOFS, the lower the available arsenic concentration although it was still higher than that of the control.

• Economic and Environmental Geology
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• v.44 no.3
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• pp.203-215
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• 2011

Geochemical and mineralogical properties of a contamited soil should be taken into account to decide a remediation strategy for a given contaminant because development and optimization of soil remedial technologies are based on geochemical and mineralogical separation techniques. The objective of this study was to investigate the geochemical and mineralogical characteristics of arsenic-contaminated soils. The arsenic-contaminated soil samples were obtained from Chonam gold mine, Gwangyang, Chonnam, Particle size analysis, sequential extraction, and mineralogical analyses were used to characterize geochemical and mineralogical characteristics of the As-contaminated soils. Particle size analyses of the As-contaminated soils showed the soils contained 17-36% sand, 25-54% silt, 9-28% clay and the soil texture were sandy loam, loam, and silt loam. The soil pH ranged from 4.5 to 6.6. The amount of arsenic concentrations from the sequential soil leaching is mainly associated with iron oxides (1 to 75%) and residuals (12 to 91%). Major minerals of sand and silt fractions in the soils were feldspar, kaolinite, mica, and quartz and minor mineral of which is an iron oxide. Major minerals of clay fraction were composed of illite, kaolinite, quartz, and vermiculite. And minor minerals are iron oxide and rutile. The geochemical and mineralogical analyses indicated the arsenic is adsorbed or coprecipitated with iron oxides or phyllosilicate minerals. The results may provide understanding of geochemical and mineralogical characteristics for the site remediation of arsenic-contaminated soils.

• Economic and Environmental Geology
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• v.43 no.4
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• pp.305-314
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• 2010

The stabilization process using limestone ($CaCO_3$) and steel making slag as the immobilization amendments was investigated for As contaminated farmland soils around Chonam abandoned mine, Korea. Batch and continuous column experiments were performed to quantify As-immobilization efficiency in soil and the analyses using XRD and SEM/EDS for secondary minerals precipitated in soil were also conducted to understand the mechanism of Asimmobilization by the amendments. For the batch experiment, with 3% of limestone and steel making slag, leaching concentration of As from the contaminated soil decreased by 62% and 52% respectively, compared to that without the amendment. When the mixed amendment (2% of limestone and 1% of steel making slag) was used, As concentration in the effluent solution decreased by 72%, showing that the mixed of limestone and steel making slag has a great capability to immobilize As in the soil. For the continuous column experiments without the amendment, As concentration from the effluent of the column ranged from 50 to $80\;{\mu}g/L$. However, with 2% limestone and 1% steel making slag, more than 80% diminution of As leaching concentration occurred within 1 year and maintained mostly below $10\;{\mu}g/L$. Results from XRD and SEM/EDS analysis for the secondary minerals created from the reaction of the amendments with $As^{+3}$ (arsenite) investigated that portlandite ($Ca(OH)_2$), calcium-arsenite (Ca-As-O) and calcite ($CaCO_3$) were main secondary minerals and the distinct As peaks in the EDS spectra of the secondary minerals can be observed. These findings suggest that the co-precipitation might be the major mechanisms to immobilize As in the soil medium with limestone and steel making slag.

• Economic and Environmental Geology
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• v.37 no.1
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• pp.121-131
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• 2004

Removal efficiencies of soil washing and soil improvement processes to remediate farmland soils and stream deposits around Goro abandoned mine were investigated with batch and column experiments. For As-contaminated farm-land soils around Goro mine, batch tests to quantify As extraction rate from contaminated soils and lime treated contaminated soils were performed. The contaminated soil mixed with lime decreased As extraction rate less than one fourth, suggesting that the soil improvement method mixed with lime dramatically decrease As extraction rate. A storage dam will be constructed in the lower part of the main stream connected to Goro abandoned mine and the amount of As extracted from the bottom soils of reservoir could be the main source to contaminate water of reservoir. The decrease of As extraction amount from the bottom in reservoir, caused by the application of the soil improvement method was investigated from the physically simulated column experiment and results showed that As extraction rate decreased to one forty when 1％ lime mixed soil improvement was applied to contaminated soils. For contaminated stream deposits connected Goro mine, the removal efficiency of the soil washing method was investigated with batch experiments. Hydrochloric acid, citric acid, acetic acid and distilled water were used as soil washing solution and 0.01, 0.05, 0.1, 0.5, 1.0 N of washing solution were applied to extract As. When washing with 0.05 N of hydrochloric acid or citric acid, more than 99.9% of As was removed from stream deposits, suggesting that As contaminated stream deposits around Goro mine be successfully remediated with the soil washing process. Total volumes of contaminated soils and deposits needed for remediation were calculated based on three different reme-diation target concentrations and the operation cost of soil washing for calculated soil volumes was estimated. Results from this research could be directly used to make a comprehensive countermeasure to remediate contaminated area around Goro mine and also many contaminated areas similar to this research area.

• Proceedings of the KAIS Fall Conference
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• 2006.05a
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• pp.582-584
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• 2006

비소와 납으로 동시에 오염된 복합오염토양 내 중금속 고정화제(비소응집제, 인산염인)를 이용하여 불용화하고자 하였다. 고정화제를 무게비율로 각각 투입하였을 때, 비소응집제와 인산염인을 0.2wt%로 동시에 첨가한 결과가 가장 높은 고정화율을 보였다.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2005.04a
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• pp.264-267
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• 2005

플럭 형성 비소 오염토양에 대한 토양세척기법의 적용성 실험결과, 세척용액 100 mM과 500 mM의 농도에서 대상 토양에 대한 비소 용출량은 수산화나트륨이 염산보다 높은 효율을 보였으며, 농도 1000 mM의 경우에는 염산이 비교적 우세한 세척효율을 보였다. 토양오염공정시험법에 의한 세척후 토양내 잔류비소 농도의 경우, 염산이 수산화나트륨과 비슷하거나 다소 우세함을 알 수 있었다. 세척 대상 토양의 Cut-off size limit을 선정하여 토양세척시 생성되는 플럭을 제거하지 않고 반복 세척한 결과, 수산화나트륨의 농도 200 mM은 1000 mM에 비하여 잔류된 비소량이 비슷하거나 비교적 높았으며, 2가지 농도에 대하여 총 5회 반복 세척한 토양의 비소 농도는 토양환경보전법의 가지역 우려기준 농도인 6 mg/kg에 근접한 결과를 보였으나, 염산의 경우 총 5회 세척시 비소의 농도가 약 9 mg/kg으로 비소 잔류량이 보다 큼을 알 수 있었다. 플럭을 제거한 후 반복 세척시 수산화나트륨의 농도 1000 mM이 200 mM에 비하여 토양 세척효율이 증가하였으며, 1000 mM로 5회 세척시 잔류비소 농도가 가지역 우려기준 농도에 근접한 약 6.7 mg/kg이었고 염산을 이용하여 세척한 경우에는 3회 세척시 약 6.7 mg/kg 4, 5회 반복 세척시 각각 약 3.9, 3.3 mg/kg으로 가지역 우려기준에 적합한 농도조건이 됨을 알 수 있었다.

• Proceedings of the KSEEG Conference
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• 2003.04a
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• pp.89-92
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• 2003

폐금은광산 지역은 토양, 작물 및 수계와 같은 지구화학적 환경에서의 비소의 부화가 환경오염의 특성으로 나타난다. 오염지역에 대한 시료채취 지점 상부에 존재하는 암석과 토양의 풍화산물인 하상퇴적물을 대상으로 하는 연구는 이들의 해당 집수지역에 존재하는 원소들의 평균 함량을 반영하므로 환경오염평가 및 광역지구화학도의 작성에 적절한 대상 시료로 사용되어 왔다. (중략)

• Economic and Environmental Geology
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• v.44 no.3
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• pp.217-228
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• 2011

The feasibility study for the stabilization process using 5 amendments was performed to quantify As-immobilization efficiency in farmland soils around Samkwang abandoned mine, Korea. For the batch experiments, with 2% and 3% of granular lime(2-5 mm in diameter), leaching concentration of As from the soil decreased by 86% and 95% respectively, compared to that without the amendment. When 5% and 10% of granular limestone was added in the soil, As concentration decreased by 82% and 95%, showing that lime and limestone has a great capability to immobilize As in the soil. From the results of batch experiments, continuous column(15 cm in dimeter and 100 cm in length) tests using granular lime and limestone as amendments was performed. Without the amendment, As concentration from the effluent of the column ranged from 167 ${\mu}g$/L to 845 ${\mu}g$/L, which were higher than Korea Drinking Water Limit(50 ${\mu}g$/L). However, only with 1% and 2% of lime, As concentration from the column dramatically decreased by 97% for 9 years rainfall and maintained below 50 ${\mu}g$/L. With 5% of limestone and the mixed amendment(1% of lime + 2% of limestone), more than 95% diminution of As leaching from the column occurred within I year rainfall and maintained below 20 ${\mu}g$/L, suggesting that the capability of limestone to immobilize As in the farmland soil was outstanding and similar to that of lime. Results of experiments suggested that As stabilization process using limestone could be more available to immobilize As from the soil than using lime because of low pH increase and thus less harmful side effect.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2004.09a
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• pp.330-333
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• 2004

국내 폐금속광산 일대에서 비소 및 중금속의 발암 및 비발암 위해성을 근거로 복원 기준치를 설정하였다. 폐금속광산일대의 주요한 노출 경로는 부지내 폐광석과 광미로부터 직접적인 오염물 흡입과 지하수를 통한 부지내 및 외 섭취의 경로로 구분된다. 지하수의 오염원은 폐광석과 광미 침출로부터의 오염과 갱구 유출로부터의 오염 및 지질매체 자체에 의한 오염이 설정되었다. 높은 오염 수준에 대해서 높은 오염성분감소비와 폐광산일대의 다양한 배경농도로부터 복원기준치를 설정 했을때, 토양 및 지하수의 복원기준치는 비소 위해도의 영향이 매우 큰 것으로 평가되었다. 비소의 높은 독성은 복원 기준치를 매우 낮게 형성했고, 위해도가 낮은 아연과 카드늄은 높게 설정되었다. 궁극적으로 오염성분 감소비에 따른 복원기준치 설정은 오염성분의 노출 경로 차단이 복원 목표치를 현실화시킬 수 있음을 보여주었다.