• Title/Summary/Keyword: Reactive Capping

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Numerical Study of Contaminant Transport Coupled with Large Strain Consolidation

  • Lee, Jang-Guen
    • Journal of The Korean Society of Agricultural Engineers
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    • v.50 no.2
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    • pp.45-52
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    • 2008
  • Contaminant transport has been widely studied in rigid porous media, but there are some cases where a large volumetric stain occurs such as dewatering of dredged contaminated sediment, landfill liner, and in-situ capping. This paper presents a numerical investigation of contaminant transport coupled with large strain consolidation. Consolidation test was performed with contaminated sediments collected in Gary, Indiana, U.S. to obtain constitutive relationships, which are required for numerical simulations. Numerical results using CST2 show an excellent agreement with measured settlement and excess pore pressure. CST2 is then used to simulate contaminant transport during and after in-situ capping. Numerical simulations provide that transient advective flows caused by consolidation significantly increase the contaminant transport rate. In addition, the numerical simulations revealed that active capping with Reactive Core Mat (RCM) significantly decelerates consolidation-induced contaminant transport.

Applicability Assessment of Steel Slag as Reactive Capping Material for Blocking Phosphorus Release from Marine Sediment (해양 퇴적물에서 인 용출 차단을 위한 반응성 피복 소재로서 제강슬래그의 적용성 검토)

  • Jo, Sung-Wook;Park, Seong-Jik
    • Journal of The Korean Society of Agricultural Engineers
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    • v.56 no.3
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    • pp.11-17
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    • 2014
  • We investigated the applicability of steel slag as a capping material in order to minimize phosphorus(P) release into seawater. Steel slag is a byproduct from the iron and steel industries and the use of steel slag has some advantages in respect of both cost and environmental concern. P removal by steel slag were studied in a batch system with respect to changes in contact time and initial concentration. Kinetic adsorption data were described well by pseudo 2nd order model, indicating rate limiting step for P adsorption to steel slag is chemical sorption. Equilibrium adsorption data fitted well to Langmuir isotherm model which describes for single layer adsorption. The maximum P adsorption capacity of steel slag was 7.134 mg-P/L. Increasing the depth of steel slag produced a positive effect on interruption of P release. More than 3 cm of steel slag was effective for blocking P release and 5 cm of steel slag was recommended as the depth for capping of P contaminated marine sediments. Increasing P concentration and flow rate had a negative effect on P removal ratio. It was concluded that the steel slag has a potential capping material for blocking P release from marine sediments.

Performance Evaluation of Microorganisms Immobilized Reactive Capping Materials on Elution Blocking of Organic, Nitrogen, and Phosphorus Compounds (미생물이 고정화된 반응성 피복재의 유기물, 질소 및 인 용출 차단성능 평가)

  • Park, Hyungjin;Kim, Young-Kee
    • Journal of Korean Society on Water Environment
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    • v.33 no.4
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    • pp.409-415
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    • 2017
  • This study aims to evaluate the effect of capping materials on blocking pollutant elution from contaminated sediment to water body. Experiments were carried out under conditions in which the elution rate was intensified artificially using compost with high concentration of organic compound and nutrient salts instead of sediments. Activated carbon (AC), modified activated carbon (MAC), P. putida immobilized activated carbon (PBAC) and effective microorganisms immobilized activated carbon (EBAC) were used as capping materials. Zeolite (ZT) and two kinds of commercially available microorganisms immobilized zeolite products (ZC, ZN) were used for comparison experiment. The elution rate of organic compound, nitrogen and phosphorus were compared with that of control experiment. The experiments were conducted for 56 days. Concentrations of chemical oxygen demand, total nitrogen, and total phosphorus were measured to use the comparison of release rate of organic compound, nitrogen and phosphorus. From the experimental results, AC based materials showed better performance to block the elution of organic compound and nitrogen than ZT based materials. Although ZT based materials were more effective than AC and PBAC to block phosphorus, MAC and EBAC showed the best performance of phosphorus elution blocking among the all candidate materials. In conclusion, EBAC is considered as the most effective capping materials, because organic compound, nitrogen and phosphorus will be degraded continuously by EM in the long term.

Assesment of Zeolite, Montmorillonite, and Steel Slag for Interrupting Heavy Metals Release from Contaminated Marine Sediments for Capping Thickness of Reactive materials (오염된 해양퇴적물에서 중금속 용출 차단을 위한 제올라이트, 몬모릴로나이트, 제강슬래그의 적용성 평가)

  • Kang, Ku;Kim, Young-Kee;Park, Seong-Jik
    • Journal of Navigation and Port Research
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    • v.39 no.4
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    • pp.335-344
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    • 2015
  • This study aims to assess the effectiveness of zeolite, montmorillonite, and steel slag as capping materials to block the release of heavy metals from marine sediment depending on their depths. The results showed that all capping materials used this study were not effective in interrupting release of As. Zeolite had negative effect on the block of Cr release but it was significantly reduced to 5 cm by montmorillonite capping. In contrast to As and Cr, Cd, Ni, and Pb were not released even from uncapped sediments. Cu and Zn were the heavy metals those were most significantly influenced by the capping conditions. Cu release from marine sediments were effectively blocked by more than 1 cm depth of montmorillonite and more than 3 cm depth of zeolite. All capping materials were found to be effective in interrupting release of Zn from marine sediments. It was concluded that the zeolite, montmorillonite, and steel slag could be used as a potential capping material for interrupting the release of Cr, Cu, and Zn from the contaminated marine sediments.

Application of Montmorillonite as Capping Material for Blocking of Phosphate Release from Contaminated Marine Sediment (해양오염퇴적물 내 인산염 용출차단을 위한 피복소재로서의 몬모릴로나이트 적용)

  • Kang, Ku;Kim, Young-Kee;Hong, Seong-Gu;Kim, Han-Joong;Park, Seong-Jik
    • Journal of Korean Society of Environmental Engineers
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    • v.36 no.8
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    • pp.554-560
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    • 2014
  • To investigate the applicability of montmorillonite to capping material for the remediation of contaminated marine sediment, adsorption characteristics of $PO{_4}{^{3-}}$ onto montmorillonite were studied in a batch system with respect to changes in contact time, initial concentration, pH, adsorbent dose amount, competing anions, adsorbent mixture, and seawater. Sorption equilibrium reached in 1 h at 50 mg/L but 3 h was required to reach sorption equilibrium at 300 mg/L. Freundlich model was more suitable to describe equilibrium sorption data than Langmuir model. The $PO{_4}{^{3-}}$ adsorption decreased as pH increased, due to the $PO{_4}{^{3-}}$ competition for favorable adsorption site with OH- at higher pH. The presence of anions such as nitrate, sulfate, and bicarbonate had no significant effect on the $PO{_4}{^{3-}}$ adsorption onto the montmorillonite. The use of the montmorillonite alone was more effective for the removal of the $PO{_4}{^{3-}}$ than mixing the montmorillonite with red mud and steel slag. The $PO{_4}{^{3-}}$ adsorption capacity of the montmorillonite was higher in seawater than deionized water, resulting from the presence of calcium ion in seawater. The water tank elution experiments showed that montmorillonite capping blocked well the elution of $PO{_4}{^{3-}}$, which was not measured up to 14 days. It was concluded that the montmirillonite has a potential capping material for the removal of the $PO{_4}{^{3-}}$ from the aqueous solutions.

Application of Lime Stone, Sand, and Zeolite as Reactive Capping Materials for Marine Sediments Contaminated with Organic Matters and Nutrients (유기물 및 영양염류로 오염된 해양퇴적물 정화를 위한 석회석, 모래, 제올라이트의 반응성 피복 소재로서 적용성 평가)

  • Kang, Ku;Park, Seong-Jik
    • Journal of Korean Society of Environmental Engineers
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    • v.39 no.8
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    • pp.470-477
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    • 2017
  • In this study, the applicability of calcite, sand, and zeolite for the remediation of sediments contaminated with organics and nutrients were investigated. Sediments and seawater for water tank experiments were sampled from Pyeongtaek harbor, and 1 cm or 3 cm of calcite, sand, and zeolite were capped on the sampled sediments. pH, electric conductivity (EC), dissolved oxygen (DO), chemical oxygen demand (COD), total nitrogen (TN), and total phosphorus (TP) were monitored for 63 days. The sampled sediments were highly contaminated with organic matter and total nitrogen. DO in uncapped condition was exhausted within 10 days but DO in capping condition except 3 cm of zeolite capping was prolonged above 2 mg/L. Capping efficiency for interrupting COD release from sediments was in the following order: zeolite 1 cm > calcite 1 cm > calcite 3 cm > sand 3 cm ${\cong}$ zeolite 3 cm ${\cong}$ sand 1 cm. Zeolite was found to be effective for interrupting nitrogen release. T-P was not observed in both uncapped and capped sediment, i.e., all experimental conditions. It can be concluded that zeolite can be effectively used for the remediation of sediments highly contaminated with organic matter and nitrogen.

Applicability of Natural Zeolite with Different Cation Exchange Capacity as In-situ Capping Materials for Adsorbing Heavy Metals (중금속 흡착을 위한 원위치 피복소재로서 천연제올라이트의 양이온교환용량에 따른 적용성 평가)

  • Kang, Ku;Shin, Weon-Ho;Hong, Seong-Gu;Kim, Young-Kee;Park, Seong-Jik
    • Journal of Korean Society of Environmental Engineers
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    • v.39 no.2
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    • pp.51-58
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    • 2017
  • We investigated the efficiency of natural zeolite with different cation exchange capacity (CEC) as capping material for the remediation of marine sediments contaminated with heavy metals. Three different zeolite with high CEC (HCzeo, 163.74 cmolc/kg), medium CEC (MCzeo, 127.20 cmolc/kg), and low CEC (LCzeo, 70.62 cmolc/kg) were used. The surface area of the zeolite was in decreasing order: HCzeo ($59.43m^2/g$) > MCzeo ($52.10m^2/g$) > LCzeo ($10.12m^2/g$). The results of mineralogical composition obtained from X-ray diffraction (XRD) show that LCzeo was mainly composed of quartz and albite. In the XRD result of MCzeo and HCzeo, the peaks of clinoptilolite, heulandite, and mordenite were also observed along with that of quartz and albite. Sorption equilibrium onto the HCzeo, MCzeo, and LCzeo was reached in 6 h at initial concentration of 10 mg/L and 100 mg/L. Higher adsorption of Cd and Zn onto the zeolite with higher CEC were achieved but adsorption of Cu and Ni were not dependent on the CEC of zeolite. It can be concluded that the zeolite with high cation exchange ability is recommended for the contaminated sediments with Cd and Zn but the inexpensive zeolite with low CEC for Cu and Ni.

Adsorption characteristics of As(III) and Cr(VI) from aqueous solution by Sediment Amendment Composite (저질개선제에 의한 수용액상의 As(III)와 Cr(VI) 흡착 특성)

  • Shin, Woo-Seok;Na, Kyu-Ri;Kim, Young-Kee
    • Journal of Korean Society on Water Environment
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    • v.32 no.2
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    • pp.216-221
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    • 2016
  • The adsorption characteristics of mixed heavy metals (Cr(III), As(VI)) in aqueous solution were investigated using a sediment amendment composite. Sediment amendment composite was composed of clean sediment (40%), zeolite (20%), recycled aggregate (10%), steel slag (10%), oyster shell (10%), and cement (10%). The experimental results showed that the adsorption equilibrium was attained after 180 mins. Heavy metal adsorption was characterized using Freundlich and Langmuir equations. The equilibrium adsorption data for the sediment amendment composite better fitted with the Langmuir model than the Freundlich model. The maximum adsorption capacity of Cr(VI) (36.07 mg/g) was higher than As(III) (25.54 mg/g); and the adsorption efficiency of the Cr(VI) and As(III) ions solution decreased with decreasing pH from 2 to 10. The collective results suggested that the sediment amendment composite is a promising material for a reactive cap that controls the release of Cr(VI) and As(III) from contaminated sediments.