• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2002.04a
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• pp.283-286
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• 2002

유류로 오염된 부지에 토양세정기법을 적용하기 위한 전 단계로, 실험실 규모의 컬럼실험을 통하여 pilot 규모 현장 적용을 위한 설계인자 및 최적 운전조건을 규명하고자 적정 세척제 종류와 농도, 배합비 및 세정용액 주입유량을 고찰하였다. 회분식실험 결과 POE$_{14}$와 SDS(1:1)를 1%로 적용한 흔합계면활성제의 효율이 가장 우수하였으나, 예비실험 결과 음이온계 계면활성제인 SDS는 미생물에 독성을 끼치는 경향이 있는 것으로 나타나 같은 농도에서 효율이 거의 유사한 POE$_{5}$와 POE$_{14}$ 혼합계면활성제를 이용하여 실험하였다. 선정된 혼합계면활성제를 적용하여 디젤 오염토양 세척능력을 검토한 결과 세척제 농도 1%까지는 효율이 증가하다가 1% 이상의 농도에서는 다시 감소하는 경향을 나타내었으며, 계면활성제 배합비는 1:1로 혼합하였을 경우 세척효율이 가장 우수하였다. 따라서 POE$_{5}$와 POE$_{14}$ (1:1) 1% 혼합계면활성제를 세척제로 선정하였다. 컬럼실험 결과, 주입 flux가 클수록 세정 제거된 총 유류의 양이 증가하였으며, 같은 pore volume의 세정용액 통과 시에는 flux가 작을수록 제거효율이 좋았다.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2003.04a
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• pp.141-144
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• 2003

청양 및 서보광산에서 채취한 광미 및 오염된 토양에 대한 산성비를 고려한 용출실험 결과, 아연, 카드뮴 및 망간 pH 6.2-5.8, 철 pH 5.2-3.2, 코발트 pH 4.4-3.2, 구리 pH 3.2-3.0, 납과비소 pH3.0-3.5의 용출조건에서 최초로 각 원소의 용출이 발생하였다. 반응용액의 최종 pH5.0-1.5사이에서 용출되는 중금속은 이온교환형태 및 탄산염광물형태와 수반된 것이 용해된 것이다. 반응용액의 최종 pH1.5이하에서 용출되는 중금속은 철과 밀접하게 수반된 것으로 해석되었다. 청양광산과 서보광산의 광미가 pH2.0이하로 유지되는 경우가 발생한다면, 청양광산은 비소(최대 6,006$\mu\textrm{g}$/g), 아연(최대 2,503$\mu\textrm{g}$/g) 및 납(최대 29,638$\mu\textrm{g}$/g), 서보광산은 납(최대 2,258$\mu\textrm{g}$/g)과 111소(최대 874$\mu\textrm{g}$/g)의 오염확산이 크게 우려되며, 이 결과는 광미에 대한 환경복원이 필요한 것을 지시한다. 서보광산의 오염된 토양은 pH3.0까지의 산성비와 반응하는 경우에는 중금속의 오염확산이 거의 우려되지 않으며, pH3.0이하의 강산 용액과 반응한다면 아연의 오염확산이 우려된다.

• Korean Journal of Soil Science and Fertilizer
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• v.24 no.2
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• pp.124-129
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• 1991

A mass balance method which measures directly both the sorbed pesticide and equilibrium solution concentration was compared with the batch method in a hypothetical experiment to determine the precision of sorption measurement. The mass balance method was shown to improve precision of sorption measurement. The two methods were also tested experimentally on the Wahiawa soil, 0-20, 40-60 and 100-120 cm, and Salinas soil, 0-15 and 115-130 cm. The mass balance method greatly improved precision of sorption measurement on the deep Wahiawa subsoil having the lowest sorption. The coefficient of variation (CV) for $K_d$ measurement was 20.3% for the batch method and 8.4% for the mass balance method. For other soil samples tested, precision of the batch method was relatively high but was still improved by the mass balance method.

• Korean Journal of Environmental Agriculture
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• v.3 no.2
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• pp.16-22
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• 1984

This study was carried out to investigate the stability of dinobuton (2-sec-butyl-4,6-dinitrophenyl isopropyl carbonate) in distilled water and buffer solutions and its persistence in soils. When dinobuton was incubated at $30^{\circ}C$ and $60^{\circ}C$ in distilled water, the half-lives of dinobuton was 28 and 6 days, respectively. The decomposition of dinobuton was, therefore, faster at high temperature than at low temperature. The half-life of dinobuton was about 27 days in the acidic solution $(pH\; 4{\sim}6)$, whereas 10 and 4 days in the alkaline solutions of pH 9, and 10, respectively. Thus dinobuton was stable in acidic solution, and unstable in alkaline solution. Dinoseb (2-sec-butyl-4,6-dinitrophenol), which is produced in the degradation process of dinobuton, was produced in small amounts in distilled water and buffer solutions. The half-life of dinobuton in sterilized soil was about 16 days longer than in non-sterilized soil. Dinoseb was also more persistent in sterilized soil than in non-sterilized one.

• Korean Journal of Environmental Agriculture
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• v.37 no.1
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• pp.21-27
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• 2018

BACKGROUND: Although 1 M $NH_4OAc$ (pH 7.0) is predominantly used as the extractant of exchangeable cations in agricultural soils, this method is unsuitable for extracting the cations in saline and calcareous soils. This study was performed to select a proper method to determine exchangeable cations in vinyl greenhouse soils. METHODS AND RESULTS: Exchangeable cations (Ca, Mg, K, Na) in saline vinyl greenhouse soils were determined after extraction with 1 M $NH_4OAc$ (pH 7.0 and 8.5) and 1 M alcoholic $NH_4Cl$ (pH 8.5). Sum of exchangeable cations of the soils extracted with 1 M $NH_4OAc$ at pH 7.0 was 1.9-2.5 times greater than soil cation exchange capaity determined at pH 7.0, even though soluble salts were pre-removed. A similar result was found when the cations were extracted with 1 M $NH_4OAc$ at pH 8.5. Those results are mostly due to the overestimation of exchangeable Ca and Mg, linked to a partial dissolution of sparingly soluble salts in $NH_4OAc$ solution. When extracted with 1 M alcoholic $NH_4Cl$ at pH 8.5, extractable Ca and Mg decreased significantly due to the lower solubility of Ca and Mg carbonates in the extractant. And the sum of exchangeable cations was very close to the corresponding exchange capacity of soils. CONCLUSION: Alcoholic $NH_4Cl$ (pH 8.5) is proposed as a reliable extractant in determination of exchangeable cations in saline vinyl greenhouse soils. And soluble salts should be removed prior to the extraction of exchangeable cations.

• Journal of Soil and Groundwater Environment
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• v.7 no.4
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• pp.77-86
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• 2002

Surfactant enhanced in-situ soil flushing was performed to remediate the soil and groundwater at an oil contaminated site, where had been used as a military vehicle repair area for 40 years. A section from the contaminated site (4.5 m $\times$ 4.5 m $\times$ 6.0 m) was selected for the research, which was composed of heterogeneous sandy and silt-sandy soils with average $K_d$ of 2.0$\times$$10^{-4}$cm/sec. Two percent of sorbitan monooleate (POE 20) and 0.07% of iso-prophyl alcohol were mixed for the surfactant solution and 3 pore volumes of surfactant solution were injected to remove oil from the contaminated section. Four injection wells and two extraction wells were built in the section to flush surfactant solution. Water samples taken from extraction wells and the storage tank were analyzed on a gas-chromatography (GC) for TPH concentration in the effluent with different time. Five pore volumes of solution were extracted while TPH concentration in soil and groundwater at the section were below the Waste Water Discharge Limit (WWDL). The effluent TPH concentration from wells with only water flushing was below 10 ppm. However, the effluent concentration using surfactant solution flushing increased to 1751 ppm, which was more than 170 times compared with the concentration with only water flushing. Total 18.5 kg of oil (TPH) was removed from the soil and groundwater at the section. The concentration of heavy metals in the effluent solution also increased with the increase of TPH concentration, suggesting that the surfactant enhanced in-situ flushing be available to remove not only oil but heavy metals from contaminated sites. The removal efficiency of surfactant enhanced in-situ flushing was investigated at the real contaminated site in Korea. Results suggest that in-situ soil flushing could be a successful process to remediate contaminated sites distributed in Korea.

• Journal of Environmental Impact Assessment
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• v.11 no.3
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• pp.173-187
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• 2002

토양 속에서 발생될 수 있는 용질과 용매의 복합 수송시스템을 대상으로 한 연구 중 회석상태로부터 포화상태에 이르기까지의 넓은 농도분포를 가지는 토양 용액에 적용될 수 있는 물리 화학적 이론에 입각한 지배방정식을 발표한 연구는 전무한 실정이다. 본 연구는 용매와 토양기체간 그리고 용질과 결정간의 상변화를 고려한 연립물질수지방정식을 제시하고, 여기에 타율적 대류를 포함하는 상호확산 분산수송방정식을 도입하여 대류와 확산에 관한 프럭스를 분리, 결정하는 것을 목적으로 한다. 대류 플럭스의 결정은 타율적으로 이루어지는 것이 이론적으로 타당하며, 이러한 타율적 대류 플럭스가 제공된다면 본 연구에서 제시된 지배방정식을 이용해서 토양용액의 복합수송 시스템을 범용적으로 해석, 예측할 수 있을 것으로 판단된다.

• Proceedings of the Korean Society of Soil and Groundwater Environment Conference
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• 2005.04a
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• pp.31-35
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• 2005

본 연구는 토양에 휘발유 첨가제인 MTBE와 휘발유의 주성분인 BTEX를 headspace 법에 의해 동시 분석하는 방법이다. 인산으로 pH를 2로 조절한 후 NaCl로 포화시킨 용액 5ml를 헤드스페이스 바이알에 보존제로 넣은 후 토양시료 약 2g을 이 용액에 침지시켜 시료 채취한 다음 헤드스페이스 장치에 넣고 $80^{\circ}C$에서 40분 가온하여 상부 기상의 일정량을 취해 GC-MS (SIM)으로 분석하였다. 본 분석법에 의한 검출한계는 methyl-tert-butyl ether(MTBE)와 benzene, toluene, ethylbenzene, o,m,p-xylene(BTEX)이 각각 0.1, 0.1, 0.1, 0.2, 0.1, 0.2 ng/g이었고, 직선성은 0.995이상이었으며, 재현성도 10%내외의 정밀한 값을 보였다. 실제 시료를 분석한 결과, MTBE가 3-6,993 ng/g의 농도분포를 보였고 total BTEX는 1 ng/g으로 검출되었다. 이 방법은 빠르고 정밀 정확한 분석법으로 공정시험법으로 활용가치가 높다.

• Proceedings of the KSEEG Conference
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• 2003.04a
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• pp.76-79
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• 2003

국내의 토양오염 공정시험방법에서는 Zn, Ni 추출시 산분해법에 가까운 방법을 사용하는 반면, Cd, Cu, Pb, $Cr^{6+}$ 추출시 0.1N HCl용액으로 산처리하여 1시간을 진탕한 후 이를 필터로 여과하여 분석용액을 추출하는 용출법을 사용하고 있다(환경부, 2001). 시료내에는 완충 물질이 존재하기 때문에 용출법 사용시 초기 pH 인 1(0.1N HCl)이 유지되지 않아 완충능력이 높은 토양의 경우 현재 국내 공정법상의 용출법이 중금속 오염정도를 추정하는데 적절치 않을 수 있다. (중략)

• Korean Journal of Soil Science and Fertilizer
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• v.26 no.4
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• pp.294-298
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• 1993

The relationship between pH and the activity of ferrous iron in the reduced soil under water-logging was investigated theoretically and experimentally. The results of this study revealed, contrary to hitherto assumed, that the $pH-Fe^{+{+}}$ relationship in the commonly occurring rice soils under reduced condition is close to that in $FeCO_3-CO_2-H_2O$ system, being remote from that in $Fe_3(OH)_8-H_2O$ system and $Fe(OH)_2-H_2O$ system. This indicates that the activity of ferrous iron in the reduced rice soils under water-logging is likely to be governed by $FeCO_3$, neither by $Fe_3(OH)_8$, nor by $Fe(OH)_2$.